Canonical Allele Identifier: PA658735442
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 492650

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119585.1:p.Ser346Leu
CA000974
NM_001126113.3:c.1037C>T