Canonical Allele Identifier: PA2741905333
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 2682400

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003713.3:p.Thr196Ser
CA2752212
NM_003722.5:c.587C>G
CA355753123
NM_003722.5:c.586A>T