Canonical Allele Identifier: PA2573241715
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1525868
ClinVar RCV Id: RCV002037012

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Val603Phe
CA353098673
NM_004656.4:c.1807G>T