Canonical Allele Identifier: PA913195180
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 630594

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Ser609Gly
CA353098423
NM_004656.4:c.1825A>G