Canonical Allele Identifier: PA2499268819
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1062750
ClinVar RCV Id: RCV001372502
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Ala502Gly
CA353100930
NM_004656.4:c.1505C>G