Canonical Allele Identifier: PA2499265325
Gene: NPR2 HGNC NCBI
ClinVar RCV:
RCV001296868
ClinVar Variation:
1000706
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003986.2:p.Arg318Gln
CA5051559
NM_003995.4:c.953G>A