Canonical Allele Identifier: PA200454
Gene: NPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 193262
ClinVar RCV Id: RCV000173314 RCV000768034 RCV000952311 RCV004539597
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003986.2:p.Ala22Ser
CA200453
NM_003995.4:c.64G>T