Canonical Allele Identifier: PA891861869
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 577431

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Pro71Ala
CA397845842
NM_001126114.3:c.211C>G