Canonical Allele Identifier: PA2825579996
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 2630702
ClinVar RCV Id: RCV003402493

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108451.1:p.His247Asp
CA355753775
NM_001114979.2:c.739C>G