Canonical Allele Identifier: PA2573100750
Gene: NIN HGNC NCBI

Linked Data

ClinVar Variation Id: 435996

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_891991.2:p.Arg1999His
CA7181063
NM_182946.2:c.5996G>A