Allele Registry

Canonical Allele Identifier: PA213466

Gene: ABCC8 HGNC NCBI

ClinVar RCV:

RCV000029268

RCV002243671

RCV002243672

ClinVar Variation:

35621

HGVS (amino-acid)	Matching Registered Transcripts
NP_001274103.1:p.Ile1519Ser	CA213464 NM_001287174.3:c.4556T>G