Canonical Allele Identifier: PA2825217064
Gene: NPR3 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000899.1:p.Gly35dup
CA443804161
NM_000908.4:c.99_101dup
CA1537620237
NM_000908.4:c.102_104dup