Allele Registry

Canonical Allele Identifier: PA207784

Gene: ABCC8 HGNC NCBI

ClinVar RCV:

RCV000029257

RCV000193953

RCV001388602

RCV003989301

ClinVar Variation:

35611

HGVS (amino-acid)	Matching Registered Transcripts
NP_001274103.1:p.Arg1183Gln	CA207783 NM_001287174.3:c.3548G>A