Canonical Allele Identifier: PA2825580214
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6527

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108452.1:p.Arg149Trp
CA118334
NM_001114980.1:c.445C>T