Canonical Allele Identifier: PA916030986
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 495834
ClinVar RCV Id: RCV000586584 RCV000710375 RCV000984140 RCV000763236 RCV003459457
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338226.1:p.Arg74Gln
CA5903946
NM_001351297.2:c.221G>A