Canonical Allele Identifier: PA2826733200
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1338515
ClinVar RCV Id: RCV001817886

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274103.1:p.Asp209Asn
CA379779069
NM_001287174.3:c.625G>A