Canonical Allele Identifier: PA2826734119
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2994775
ClinVar RCV Id: RCV003858398

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274103.1:p.Thr1535Asn
CA379781795
NM_001287174.3:c.4604C>A