Canonical Allele Identifier: PA658673338
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 485254

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Arg551Cys
CA2436763
NM_004656.4:c.1651C>T