Canonical Allele Identifier: PA2825580426
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 1451179
ClinVar RCV Id: RCV002007150
ClinVar Variation Id: 1475057
ClinVar RCV Id: RCV001973838

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108452.1:p.Phe471Leu
CA355759032
NM_001114980.1:c.1411T>C
CA355759040
NM_001114980.1:c.1413C>A
CA355759043
NM_001114980.1:c.1413C>G