Canonical Allele Identifier: PA2826559625
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1021934
ClinVar RCV Id: RCV001321777

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Pro151Ala
CA397840850
NM_001276695.3:c.451C>G