Canonical Allele Identifier: PA2827264897
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6544

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316075.1:p.Ile370Thr
CA118342
NM_001329146.2:c.1109T>C