Allele Registry

Canonical Allele Identifier: PA111487

Gene: AGPS HGNC NCBI

ClinVar RCV:

RCV000007024

ClinVar Variation:

6645

HGVS (amino-acid)	Matching Registered Transcripts
NP_003650.1:p.Arg419His	CA118386 NM_003659.4:c.1256G>A