Canonical Allele Identifier: PA174618
Gene: NMD3 HGNC NCBI

Linked Data

ClinVar Variation Id: 161698
ClinVar RCV Id: RCV000149234
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057022.2:p.Thr168Ile
CA174617
NM_015938.5:c.503C>T