Canonical Allele Identifier: PA1139715944
Gene: NPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 873127
ClinVar RCV Id: RCV001262118 RCV001385134 RCV001597245 RCV002283524
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003986.2:p.Thr907Met
CA373384753
NM_003995.4:c.2720C>T