Canonical Allele Identifier: PA2741902947
Gene: NRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2782439
ClinVar RCV Id: RCV003663974

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003480.2:p.Ser90Thr
CA9981519
NM_003489.4:c.268T>A