Canonical Allele Identifier: PA2826559614
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1378428
ClinVar RCV Id: RCV001881135

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Ala150Gly
CA397840857
NM_001276695.3:c.449C>G