Allele Registry

Canonical Allele Identifier: PA093138

Gene: BPGM HGNC NCBI

ClinVar RCV:

RCV000012872

RCV003556005

ClinVar Variation:

12091

HGVS (amino-acid)	Matching Registered Transcripts
NP_001280014.1:p.Arg90Cys	CA212935 NM_001293085.2:c.268C>T