Canonical Allele Identifier: PA645501132
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 412429
ClinVar RCV Id: RCV000581046 RCV000475113 RCV001552368 RCV002248694
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Ser583Leu
CA16611516
NM_004656.4:c.1748C>T