Canonical Allele Identifier: PA2580173088
Gene: NPR3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1983907
ClinVar RCV Id: RCV002770519

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191304.1:p.Val29_Gly35del
CA3222324
NM_001204375.2:c.86_106del
CA2673456117
NM_001204375.2:c.75_95del