Canonical Allele Identifier: PA658725201
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 489622

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Arg551His
CA2436762
NM_004656.4:c.1652G>A