Allele Registry

Canonical Allele Identifier: PA278611

Gene: NAGPA HGNC NCBI

ClinVar Allele:

39651

ClinVar RCV:

RCV000023672

ClinVar Variation:

30694

HGVS (amino-acid)	Matching Registered Transcripts
NP_057340.2:p.Arg328Cys	CA278610 NM_016256.4:c.982C>T