Canonical Allele Identifier: PA1139733914
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 935598
ClinVar RCV Id: RCV001204229
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Met615Leu
CA353098214
NM_004656.4:c.1843A>T
CA353098218
NM_004656.4:c.1843A>C