Allele Registry

Canonical Allele Identifier: PA213469

Gene: ABCC8 HGNC NCBI

ClinVar RCV:

RCV000029269

ClinVar Variation:

35622

HGVS (amino-acid)	Matching Registered Transcripts
NP_001274103.1:p.Val1523Met	CA213467 NM_001287174.3:c.4567G>A