Canonical Allele Identifier: PA2827281727
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6544

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316893.1:p.Ile547Thr
CA118342
NM_001329964.2:c.1640T>C