Canonical Allele Identifier: PA2825579848
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6544

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108450.1:p.Ile549Thr
CA118342
NM_001114978.2:c.1646T>C