Allele Registry

Canonical Allele Identifier: PA2827606207

Gene: ABCC8 HGNC NCBI

ClinVar RCV:

RCV000009657

RCV000029263

RCV001277179

RCV001390783

RCV002326685

RCV003321485

RCV003466873

ClinVar Variation:

35616

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338226.1:p.Gly1399Arg	CA260102 NM_001351297.2:c.4195G>A CA379787674 NM_001351297.2:c.4195G>C