Canonical Allele Identifier: PA2827264217
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6531
ClinVar RCV Id: RCV000006904

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316073.1:p.Lys233Glu
CA118337
NM_001329144.2:c.697A>G