Canonical Allele Identifier: PA916006555
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 406597

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Arg71Leu
CA002845
NM_001276761.3:c.212G>T