Allele Registry

Canonical Allele Identifier: PA151260

Gene: NPPA HGNC NCBI

ClinVar Variation Id: 126847

HGVS (amino-acid)	Matching Registered Transcripts
NP_006163.1:p.Ser64Arg	CA151258 NM_006172.4:c.190A>C CA338451241 NM_006172.4:c.192T>A CA338451243 NM_006172.4:c.192T>G