ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826560708
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000162461
RCV000237013
RCV000417610
RCV000419372
RCV000420028
RCV000421040
RCV000421688
RCV000425628
RCV000426825
RCV000427448
RCV000428519
RCV000430781
RCV000431915
RCV000432405
RCV000433024
RCV000436631
RCV000438105
RCV000438666
RCV000439150
RCV000441098
RCV000442735
RCV000443535
RCV000457119
RCV000576336
RCV003462117
ClinVar Variation:
183748
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263625.1:p.Thr86Met
CA000140
NM_001276696.3:c.257C>T