Canonical Allele Identifier: PA2826562006
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376614

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.His34Asn
CA16603035
NM_001276697.3:c.100C>A