Canonical Allele Identifier: PA2828800387
Gene: NPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 944231
ClinVar RCV Id: RCV001214587

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365852.1:p.Arg423Gln
CA5051646
NM_001378923.1:c.1268G>A