Canonical Allele Identifier: PA916030882
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 804491
ClinVar RCV Id: RCV000991471 RCV001277190 RCV001819697 RCV002488083
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338224.1:p.Thr1160Met
CA5902811
NM_001351295.2:c.3479C>T