Canonical Allele Identifier: PA2741906902
Gene: NPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2924076
ClinVar RCV Id: RCV003785826
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003986.2:p.Pro432Ser
CA373371166
NM_003995.4:c.1294C>T