Canonical Allele Identifier: PA1139733823
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 928008
ClinVar RCV Id: RCV001191656

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Gly578Val
CA353099347
NM_004656.4:c.1733G>T