Canonical Allele Identifier: PA2499268828
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1057670
ClinVar RCV Id: RCV001366698

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Ala549Thr
CA353100103
NM_004656.4:c.1645G>A