Canonical Allele Identifier: PA2579936881
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 634690

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Phe113Cys
CA397844502
NM_000546.6:c.338T>G
CA645589268
NM_000546.6:c.338_339delinsGT