Canonical Allele Identifier: PA2741918140
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2770207
ClinVar RCV Id: RCV003527939
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Lys601Asn
CA353098718
NM_004656.4:c.1803G>T
CA353098719
NM_004656.4:c.1803G>C