Canonical Allele Identifier: PA658662180
Gene: NPPA HGNC NCBI

Linked Data

ClinVar Variation Id: 469607

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006163.1:p.Gln91Arg
CA597043
NM_006172.4:c.272A>G