Canonical Allele Identifier: PA2579936613
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2121740
ClinVar RCV Id: RCV003043347

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Val122Leu
CA397844318
NM_000546.6:c.364G>T
CA397844319
NM_000546.6:c.364G>C