Canonical Allele Identifier: PA916049729
Gene: NIN HGNC NCBI

Linked Data

ClinVar Variation Id: 37291
ClinVar RCV Id: RCV000030830 RCV002513279 RCV003478979
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057434.4:p.Asn996Ser
CA130147
NM_016350.5:c.2987A>G