Allele Registry

Canonical Allele Identifier: PA2827687839

Gene: ARSG HGNC NCBI

ClinVar RCV:

RCV001230639

ClinVar Variation:

957632

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339832.1:p.Gln229His	CA400743329 NM_001352903.2:c.687G>C CA400743330 NM_001352903.2:c.687G>T