Canonical Allele Identifier: PA204427
Gene: NPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 208356
ClinVar RCV Id: RCV000190428 RCV001362476
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003986.2:p.Arg819Cys
CA204426
NM_003995.4:c.2455C>T