Canonical Allele Identifier: PA915990029
Gene: NRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 781506
ClinVar RCV Id: RCV000962746

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003480.2:p.Val37Ile
CA9981545
NM_003489.4:c.109G>A