Canonical Allele Identifier: PA2579951931
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 482226

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Phe338Leu
CA000848
NM_000546.6:c.1014C>G
CA397832711
NM_000546.6:c.1014C>A
CA397832735
NM_000546.6:c.1012T>C