Canonical Allele Identifier: PA2827606211
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1311162
ClinVar RCV Id: RCV001758671
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338226.1:p.Ile1402Thr
CA379787397
NM_001351297.2:c.4205T>C