Canonical Allele Identifier: PA2573075887
Gene: NPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 283086
ClinVar RCV Id: RCV000328406 RCV001166431 RCV001300728
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365852.1:p.Arg779Gln
CA5051937
NM_001378923.1:c.2336G>A