Canonical Allele Identifier: PA2499268858
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1039798
ClinVar RCV Id: RCV001343342

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Thr559Arg
CA353099924
NM_004656.4:c.1676C>G