Canonical Allele Identifier: PA2828800248
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_001365852.1:p.Ser76Pro
CA204428
NM_001378923.1:c.226T>C