Canonical Allele Identifier: PA220125
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 18449
ClinVar RCV Id: RCV000009655 RCV000077845
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274103.1:p.Gly716Val
CA220124
NM_001287174.3:c.2147G>T