Canonical Allele Identifier: PA2573075898
Gene: NPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 194950
ClinVar RCV Id: RCV000175437 RCV001319753
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365852.1:p.Ile911Thr
CA241195
NM_001378923.1:c.2732T>C