Allele Registry

Canonical Allele Identifier: PA2827606337

Gene: ABCC8 HGNC NCBI

ClinVar RCV:

RCV000029268

RCV002243671

RCV002243672

ClinVar Variation:

35621

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338226.1:p.Ile1517Ser	CA213464 NM_001351297.2:c.4550T>G