Canonical Allele Identifier: PA2825580676
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6529
ClinVar RCV Id: RCV000006902

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108453.1:p.Cys251Arg
CA118336
NM_001114981.1:c.751T>C