Allele Registry

Canonical Allele Identifier: PA658673362

Gene: BAP1 HGNC NCBI

ClinVar RCV:

RCV000568696

RCV001306840

RCV002264958

ClinVar Variation:

480826

HGVS (amino-acid)	Matching Registered Transcripts
NP_004647.1:p.Met615Val	CA353098219 NM_004656.4:c.1843A>G