Canonical Allele Identifier: PA645501167
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 412402
ClinVar RCV Id: RCV000458742 RCV000580496
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Pro618Ala
CA16611514
NM_004656.4:c.1852C>G