Canonical Allele Identifier: PA915979430
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 660125
ClinVar RCV Id: RCV000817260 RCV001805893
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Arg540Cys
CA74740654
NM_004656.4:c.1618C>T