Canonical Allele Identifier: PA1139733555
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 923482
ClinVar RCV Id: RCV001184191 RCV003473723
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Asn504Lys
CA353100894
NM_004656.4:c.1512C>G
CA353100896
NM_004656.4:c.1512C>A