Allele Registry

Canonical Allele Identifier: PA2499297938

Gene: ABCC11 HGNC NCBI

ClinVar RCV:

RCV001354771

ClinVar Variation:

1049104

HGVS (amino-acid)	Matching Registered Transcripts
NP_660187.1:p.Thr389Asn	CA8043982 NM_145186.3:c.1166C>A