Canonical Allele Identifier: PA2828800393
Gene: NPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 583173
ClinVar RCV Id: RCV000707442
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365852.1:p.Pro438His
CA373371237
NM_001378923.1:c.1313C>A