Allele Registry

Canonical Allele Identifier: PA2827790918

Gene: STAMBP HGNC NCBI

ClinVar RCV:

RCV001808859

RCV002074227

ClinVar Variation:

1333643

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340896.1:p.Arg38Gly	CA347303522 NM_001353967.2:c.112C>G