Canonical Allele Identifier: PA2827605973
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 446769
ClinVar RCV Id: RCV000517936 RCV002244986 RCV002274051 RCV003736800
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338226.1:p.Ala1151Val
CA379798305
NM_001351297.2:c.3452C>T