Canonical Allele Identifier: PA913195184
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 629041
ClinVar RCV Id: RCV000773729 RCV001300787 RCV001572485
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Ser623Asn
CA353098033
NM_004656.4:c.1868G>A