Canonical Allele Identifier: PA916030918
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 556207
ClinVar RCV Id: RCV000672178
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338224.1:p.Ala1388Asp
CA379790301
NM_001351295.2:c.4163C>A