Canonical Allele Identifier: PA2741902944
Gene: NRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2629219
ClinVar RCV Id: RCV003414101

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003480.2:p.Asn45Asp
CA409832978
NM_003489.4:c.133A>G