Canonical Allele Identifier: PA2579935574
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 646725

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Pro190Ser
CA397840839
NM_000546.6:c.568C>T