Canonical Allele Identifier: PA2827606338
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1312141
ClinVar RCV Id: RCV001761362

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338226.1:p.Leu1518Phe
CA379782201
NM_001351297.2:c.4552C>T