Canonical Allele Identifier: PA916030889
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 35611

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338224.1:p.Arg1204Gln
CA207783
NM_001351295.2:c.3611G>A