Canonical Allele Identifier: PA111816
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6529
ClinVar RCV Id: RCV000006902

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003713.3:p.Cys345Arg
CA118336
NM_003722.5:c.1033T>C