Canonical Allele Identifier: PA2573075897
Gene: NPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 873127
ClinVar RCV Id: RCV001262118 RCV001385134 RCV001597245 RCV002283524
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365852.1:p.Thr910Met
CA373384753
NM_001378923.1:c.2729C>T