Canonical Allele Identifier: PA2827605767
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1489024

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338226.1:p.Arg840Gly
CA379807481
NM_001351297.2:c.2518C>G