Canonical Allele Identifier: PA204429
Gene: NPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 208357
ClinVar RCV Id: RCV000190429
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003986.2:p.Ser76Pro
CA204428
NM_003995.4:c.226T>C