Canonical Allele Identifier: PA645294172
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_003986.2:p.Cys768Arg
CA16044042
NM_003995.4:c.2302T>C