Canonical Allele Identifier: PA658725217
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 489623

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Ser571Asn
CA74740568
NM_004656.4:c.1712G>A