Canonical Allele Identifier: PA2827606009
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 35611

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338226.1:p.Arg1181Gln
CA207783
NM_001351297.2:c.3542G>A