Canonical Allele Identifier: PA2827606141
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2027939
ClinVar RCV Id: RCV002863396
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338226.1:p.Tyr1352His
CA379790654
NM_001351297.2:c.4054T>C