Canonical Allele Identifier: PA645401996
Gene: NPPA HGNC NCBI

Linked Data

ClinVar Variation Id: 415936
ClinVar RCV Id: RCV000469485

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006163.1:p.Gly98Arg
CA597036
NM_006172.4:c.292G>A
CA338450248
NM_006172.4:c.292G>C