Canonical Allele Identifier: PA2741819801
Gene: NPR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2547188
ClinVar RCV Id: RCV004321246

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000897.3:p.Asp467Glu
CA342521900
NM_000906.4:c.1401T>A
CA342521901
NM_000906.4:c.1401T>G