Canonical Allele Identifier: PA2827604033
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 21168
ClinVar RCV Id: RCV000020289
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338225.1:p.Asp209Glu
CA341691
NM_001351296.2:c.627C>A
CA379779047
NM_001351296.2:c.627C>G