Canonical Allele Identifier: PA2741902955
Gene: NRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3061374
ClinVar RCV Id: RCV003983382
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003480.2:p.Asp196Glu
CA409831965
NM_003489.4:c.588T>G
CA409831966
NM_003489.4:c.588T>A