Canonical Allele Identifier: PA2573075911
Gene: NPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91957
ClinVar RCV Id: RCV000122514
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365852.1:p.Gln1019His
CA232240
NM_001378923.1:c.3057G>T
CA373386819
NM_001378923.1:c.3057G>C