Canonical Allele Identifier: PA2828800306
Gene: NPR2 HGNC NCBI
ClinVar RCV:
RCV002044356
ClinVar Variation:
1348509
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365852.1:p.Phe253del
CA5051508
NM_001378923.1:c.756_758del