Canonical Allele Identifier: PA2580285397
Gene: NRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2377630
ClinVar RCV Id: RCV002674140
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003480.2:p.His27Arg
CA9981550
NM_003489.4:c.80A>G