Canonical Allele Identifier: PA658662186
Gene: NPPA HGNC NCBI

Linked Data

ClinVar Variation Id: 469608
ClinVar RCV Id: RCV000541350

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006163.1:p.Ser142Asn
CA597006
NM_006172.4:c.425G>A