Canonical Allele Identifier: PA2499268827
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1045137

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Ile544Val
CA353100193
NM_004656.4:c.1630A>G