Canonical Allele Identifier: PA2827264307
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6541

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316073.1:p.Asp351Gly
CA118341
NM_001329144.2:c.1052A>G