Canonical Allele Identifier: PA916030928
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_001338224.1:p.Ser1404Arg
CA10588932
NM_001351295.2:c.4212T>G
CA379788276
NM_001351295.2:c.4212T>A
CA379788302
NM_001351295.2:c.4210A>C