Canonical Allele Identifier: PA2827604717
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1338431
ClinVar RCV Id: RCV001817802 RCV003321874 RCV004526149
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338225.1:p.His1097Pro
CA379801444
NM_001351296.2:c.3290A>C