Canonical Allele Identifier: PA2580308760
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1781231
ClinVar RCV Id: RCV002412918
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Met615Ile
CA353098207
NM_004656.4:c.1845G>T
CA353098208
NM_004656.4:c.1845G>C
CA353098209
NM_004656.4:c.1845G>A