Canonical Allele Identifier: PA2829465262
Gene: NRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3202140
ClinVar RCV Id: RCV004493552

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003480.2:p.Met119Leu
CA9981510
NM_003489.4:c.355A>T
CA409832484
NM_003489.4:c.355A>C