Canonical Allele Identifier: PA2573075885
Gene: NPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 375291
ClinVar RCV Id: RCV000416364
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365852.1:p.Cys771Arg
CA16044042
NM_001378923.1:c.2311T>C