Canonical Allele Identifier: PA2499265320
Gene: NPR2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003986.2:p.Arg218Trp
CA5051480
NM_003995.4:c.652C>T