ClinGen Allele Registry
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Canonical Allele Identifier:
PA2825605564
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
376593
ClinVar RCV Id:
RCV000419358
RCV000421888
RCV000421331
RCV000423414
RCV000424971
RCV000427672
RCV000430190
RCV000431576
RCV000433092
RCV000434375
RCV000439537
RCV000437905
RCV000443500
RCV000443287
RCV000444095
RCV004022212
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001119585.1:p.Glu286Ala
CA16603015
NM_001126113.3:c.857A>C