Canonical Allele Identifier: PA2829864497
Gene: NIN HGNC NCBI

Linked Data

ClinVar Variation Id: 435996

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057434.4:p.Arg1286His
CA7181063
NM_016350.5:c.3857G>A