Canonical Allele Identifier: PA2827605085
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 9096
ClinVar RCV Id: RCV000009664 RCV000710390 RCV001831558 RCV004549354 RCV003466844
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338225.1:p.Arg1493Trp
CA254633
NM_001351296.2:c.4477C>T