Canonical Allele Identifier: PA2579937031
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 492752

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Ser106Arg
CA397844688
NM_000546.6:c.318C>G
CA397844691
NM_000546.6:c.318C>A
CA397844720
NM_000546.6:c.316A>C