Canonical Allele Identifier: PA2573232714
Gene: NPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1348509
ClinVar RCV Id: RCV002044356
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003986.2:p.Phe253del
CA5051508
NM_003995.4:c.756_758del