Canonical Allele Identifier: PA2827605639
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2083868
ClinVar RCV Id: RCV003002828

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338226.1:p.Asp672Asn
CA5903346
NM_001351297.2:c.2014G>A