Canonical Allele Identifier: PA645401985
Gene: NPPA HGNC NCBI

Linked Data

ClinVar Variation Id: 410071
ClinVar RCV Id: RCV000460903

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006163.1:p.Val58Met
CA597072
NM_006172.4:c.172G>A