Canonical Allele Identifier: PA2825579969
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 1391041
ClinVar RCV Id: RCV001910897
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108451.1:p.Val224Leu
CA355753419
NM_001114979.2:c.670G>C