Canonical Allele Identifier: PA113001
Gene: NPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2925447
ClinVar RCV Id: RCV003781101
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003986.2:p.Thr297Met
CA373369142
NM_003995.4:c.890C>T