Canonical Allele Identifier: PA2825613518
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
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119588.1:p.Cys106Gly
CA16603003
NM_001126116.1:c.316T>G