Canonical Allele Identifier: PA2573071021
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1339207

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338224.1:p.Asp1376Asn
CA379790603
NM_001351295.2:c.4126G>A