Canonical Allele Identifier: PA2828800231
Gene: NPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 193262
ClinVar RCV Id: RCV000173314 RCV000768034 RCV000952311 RCV004539597
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365852.1:p.Ala22Ser
CA200453
NM_001378923.1:c.64G>T