Canonical Allele Identifier: PA645438575
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 265022

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274103.1:p.Lys1344Met
CA10588515
NM_001287174.3:c.4031A>T