Canonical Allele Identifier: PA2825580414
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6535
ClinVar RCV Id: RCV000006909

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108452.1:p.Leu459Phe
CA253874
NM_001114980.1:c.1377A>T
CA355758874
NM_001114980.1:c.1377A>C