Canonical Allele Identifier: PA2825605684
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1332597
ClinVar RCV Id: RCV001805643

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119585.1:p.Pro301Ala
CA397836355
NM_001126113.3:c.901C>G