Canonical Allele Identifier: PA915997784
Gene: NDN HGNC NCBI

Linked Data

ClinVar Variation Id: 713375
ClinVar RCV Id: RCV000885505
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002478.1:p.Pro88Leu
CA7430281
NM_002487.3:c.263C>T