Canonical Allele Identifier: PA2830397972
Gene: NIN HGNC NCBI

Linked Data

ClinVar Variation Id: 37291
ClinVar RCV Id: RCV000030830 RCV002513279 RCV003478979
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_891991.2:p.Asn1709Ser
CA130147
NM_182946.2:c.5126A>G