Canonical Allele Identifier: PA2573232799
Gene: NPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1402358
ClinVar RCV Id: RCV001906398
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003986.2:p.Thr421Met
CA5051643
NM_003995.4:c.1262C>T