Canonical Allele Identifier: PA1139734021
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 864327
ClinVar RCV Id: RCV001071482 RCV001760057 RCV002411621
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Pro621Thr
CA353098088
NM_004656.4:c.1861C>A