Allele Registry

Canonical Allele Identifier: PA2573075888

Gene: NPR2 HGNC NCBI

ClinVar RCV:

RCV001733607

RCV002032734

ClinVar Variation:

1301658

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365852.1:p.Arg779Trp	CA373379257 NM_001378923.1:c.2335C>T