Canonical Allele Identifier: PA2829938031
Gene: NIN HGNC NCBI

Linked Data

ClinVar Variation Id: 435996

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065972.4:p.Arg1999His
CA7181063
NM_020921.4:c.5996G>A