Canonical Allele Identifier: PA2828800336
Gene: NPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1377064
ClinVar RCV Id: RCV001889819
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365852.1:p.Arg312His
CA5051553
NM_001378923.1:c.935G>A