Canonical Allele Identifier: PA112970
Gene: NPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 17786
ClinVar RCV Id: RCV000019364
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003986.2:p.Asp176Glu
CA250694
NM_003995.4:c.528T>A
CA373364775
NM_003995.4:c.528T>G