Allele Registry

Canonical Allele Identifier: PA2828434338

Gene: ABCC11 HGNC NCBI

ClinVar RCV:

RCV001354500

ClinVar Variation:

1048993

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357425.1:p.Ala286Thr	CA8044073 NM_001370496.1:c.856G>A