Canonical Allele Identifier: PA2825580198
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 730540
ClinVar RCV Id: RCV001513730

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108452.1:p.Ile131Val
CA2752223
NM_001114980.1:c.391A>G