Canonical Allele Identifier: PA106882
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376577
ClinVar RCV Id: RCV000417486 RCV000420677 RCV000422283 RCV000422044 RCV000423396 RCV000427246 RCV000428804 RCV000428630 RCV000430919 RCV000433478 RCV000435170 RCV000437321 RCV000437476 RCV000438876 RCV000439946 RCV000443356 RCV000444792 RCV000785550 RCV001390630 RCV002365460
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Cys238Gly
CA16603003
NM_000546.6:c.712T>G