Allele Registry

Canonical Allele Identifier: PA916030960

Gene: ABCC8 HGNC NCBI

ClinVar RCV:

RCV000029269

ClinVar Variation:

35622

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338224.1:p.Val1544Met	CA213467 NM_001351295.2:c.4630G>A