Allele Registry

Canonical Allele Identifier: PA269942

Gene: ABCC1 HGNC NCBI

ClinVar RCV:

RCV000123404

ClinVar Variation:

126859

HGVS (amino-acid)	Matching Registered Transcripts
NP_004987.2:p.Arg723Gln	CA269941 NM_004996.4:c.2168G>A