Canonical Allele Identifier: PA2580308763
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1781371
ClinVar RCV Id: RCV002413058 RCV003100890
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Pro618Leu
CA353098156
NM_004656.4:c.1853C>T