Canonical Allele Identifier: PA2580308639
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2129133
ClinVar RCV Id: RCV003057924

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Ala502Asp
CA353100933
NM_004656.4:c.1505C>A