Canonical Allele Identifier: PA645294174
Gene: NPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 283086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003986.2:p.Arg776Gln
CA5051937
NM_003995.4:c.2327G>A