Allele Registry

Canonical Allele Identifier: PA212937

Gene: BPGM HGNC NCBI

ClinVar RCV:

RCV000012872

RCV003556005

ClinVar Variation:

12091

HGVS (amino-acid)	Matching Registered Transcripts
NP_954655.1:p.Arg90Cys	CA212935 NM_199186.3:c.268C>T