Canonical Allele Identifier: PA658673330
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 472673
ClinVar RCV Id: RCV000530202
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Leu539Pro
CA353100288
NM_004656.4:c.1616T>C