Canonical Allele Identifier: PA2825217088
Gene: NPR3 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000899.1:p.Glu54Gln
CA359466304
NM_000908.4:c.160G>C