Canonical Allele Identifier: PA207784
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 35611

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274103.1:p.Arg1183Gln
CA207783
NM_001287174.3:c.3548G>A