Allele Registry

Canonical Allele Identifier: PA3057559680

Gene: ABCC8 HGNC NCBI

ClinVar Allele:

3720033

ClinVar RCV:

RCV005046582

ClinVar Variation:

3599370

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338226.1:p.Ala769Gly	CA379809694 NM_001351297.2:c.2306C>G