Allele Registry

Canonical Allele Identifier: PA2830088292

Gene: ABCC11 HGNC NCBI

ClinVar RCV:

RCV001354771

ClinVar Variation:

1049104

HGVS (amino-acid)	Matching Registered Transcripts
NP_115972.2:p.Thr389Asn	CA8043982 NM_032583.4:c.1166C>A