Canonical Allele Identifier: PA916030967
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 188836

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338224.1:p.Leu1565Pro
CA274017
NM_001351295.2:c.4694T>C