Canonical Allele Identifier: PA2828800281
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_001365852.1:p.Asp176Glu
CA250694
NM_001378923.1:c.528T>A
CA373364775
NM_001378923.1:c.528T>G