Canonical Allele Identifier: PA2580282505
Gene: NPR2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003986.2:p.Ile223Ser
CA5051497
NM_003995.4:c.668T>G