Canonical Allele Identifier: PA2827605673
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 18449
ClinVar RCV Id: RCV000009655 RCV000077845
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338226.1:p.Gly715Val
CA220124
NM_001351297.2:c.2144G>T