Canonical Allele Identifier: PA2741902954
Gene: NRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2888164
ClinVar RCV Id: RCV003724733
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003480.2:p.Lys195Arg
CA317655728
NM_003489.4:c.584A>G