Canonical Allele Identifier: PA2827604035
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 21169
ClinVar RCV Id: RCV000020290 RCV003556056
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338225.1:p.Gln211Lys
CA341693
NM_001351296.2:c.631C>A