Canonical Allele Identifier: PA658673347
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 485292
ClinVar RCV Id: RCV000649801 RCV000565092 RCV003318599
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Gln593Arg
CA353098947
NM_004656.4:c.1778A>G