Canonical Allele Identifier: PA2828800382
Gene: NPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 208360
ClinVar RCV Id: RCV000190432 RCV002514081
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365852.1:p.Gln417Glu
CA204434
NM_001378923.1:c.1249C>G