Canonical Allele Identifier: PA2825610647
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376690
ClinVar RCV Id: RCV000421263 RCV000421924 RCV000423467 RCV000427293 RCV000430039 RCV000430207 RCV000431511 RCV000433051 RCV000437540 RCV000439556 RCV000440245 RCV000444569 RCV000443862 RCV000444596 RCV001025931 RCV001341542
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119587.1:p.Tyr102Ser
CA16603103
NM_001126115.1:c.305A>C