Canonical Allele Identifier: PA916030984
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 9107

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338226.1:p.Asn72Ser
CA340870
NM_001351297.2:c.215A>G