Allele Registry

Canonical Allele Identifier: PA645501126

Gene: BAP1 HGNC NCBI

ClinVar RCV:

RCV000461126

RCV000579418

ClinVar Variation:

412442

HGVS (amino-acid)	Matching Registered Transcripts
NP_004647.1:p.Arg518Trp	CA2436776 NM_004656.4:c.1552C>T CA3057227412 NM_004656.4:c.1551_1552delinsCT