Canonical Allele Identifier: PA2579936912
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376631
ClinVar RCV Id: RCV000420444 RCV000423328 RCV000423948 RCV000429869 RCV000430499 RCV000435486 RCV000440112 RCV000441661 RCV003509528
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Leu111Arg
CA16603050
NM_000546.6:c.332T>G