Canonical Allele Identifier: PA2828800339
Gene: NPR2 HGNC NCBI
ClinVar RCV:
RCV001296868
ClinVar Variation:
1000706
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365852.1:p.Arg318Gln
CA5051559
NM_001378923.1:c.953G>A