Canonical Allele Identifier: PA2827604959
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 265990
ClinVar RCV Id: RCV000256388
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338225.1:p.Ser1382Arg
CA10588932
NM_001351296.2:c.4146T>G
CA379788276
NM_001351296.2:c.4146T>A
CA379788302
NM_001351296.2:c.4144A>C