Canonical Allele Identifier: PA2827606143
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1339207

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338226.1:p.Asp1353Asn
CA379790603
NM_001351297.2:c.4057G>A