Canonical Allele Identifier: PA916030931
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 157701
ClinVar RCV Id: RCV000144999
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338224.1:p.Phe1414Val
CA233277
NM_001351295.2:c.4240T>G