Canonical Allele Identifier: PA2829937926
Gene: NIN HGNC NCBI

Linked Data

ClinVar Variation Id: 37291

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065972.4:p.Asn1709Ser
CA130147
NM_020921.4:c.5126A>G