Allele Registry

Canonical Allele Identifier: PA2827606340

Gene: ABCC8 HGNC NCBI

ClinVar RCV:

RCV000029269

ClinVar Variation:

35622

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338226.1:p.Val1521Met	CA213467 NM_001351297.2:c.4561G>A