Canonical Allele Identifier: PA2499268834
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1055807

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Gly581Asp
CA353099295
NM_004656.4:c.1742G>A