ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA186309
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
183748
ClinVar RCV Id:
RCV000162461
RCV000237013
RCV000421040
RCV000417610
RCV000428519
RCV000426825
RCV000433024
RCV000441098
RCV000420028
RCV000457119
RCV000419372
RCV000421688
RCV000425628
RCV000430781
RCV000427448
RCV000431915
RCV000432405
RCV000436631
RCV000438666
RCV000438105
RCV000439150
RCV000442735
RCV000443535
RCV000576336
RCV003462117
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001119585.1:p.Thr125Met
CA000140
NM_001126113.3:c.374C>T