Canonical Allele Identifier: PA2827605917
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1034174
ClinVar RCV Id: RCV001336813
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338226.1:p.Ser1052Asn
CA5902908
NM_001351297.2:c.3155G>A