Canonical Allele Identifier: PA2573232750
Gene: NPR2 HGNC NCBI
ClinVar RCV:
RCV001889819
ClinVar Variation:
1377064
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003986.2:p.Arg312His
CA5051553
NM_003995.4:c.935G>A