Canonical Allele Identifier: PA2827603053
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 9107

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338224.1:p.Asn72Ser
CA340870
NM_001351295.2:c.215A>G