Canonical Allele Identifier: PA2573075908
Gene: NPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 418389
ClinVar RCV Id: RCV000480765 RCV000985136 RCV002469165 RCV003766658
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365852.1:p.Arg992Leu
CA16618861
NM_001378923.1:c.2975G>T