Canonical Allele Identifier: PA2573075891
Gene: NPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 423845
ClinVar RCV Id: RCV000487025
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365852.1:p.Arg851Trp
CA5052002
NM_001378923.1:c.2551C>T