Canonical Allele Identifier: PA2825580421
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6536

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108452.1:p.Cys467Gly
CA253875
NM_001114980.1:c.1399T>G