Canonical Allele Identifier: PA916030972
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 495835
ClinVar RCV Id: RCV000588969 RCV000666072 RCV001386147 RCV002491164 RCV001829617 RCV003459458 RCV004545790
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338226.1:p.Val21Asp
CA5903992
NM_001351297.2:c.62T>A