Canonical Allele Identifier: PA2573166334
Gene: NDP HGNC NCBI

Linked Data

ClinVar Variation Id: 1486323
ClinVar RCV Id: RCV002003509
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000257.1:p.Arg38His
CA413009085
NM_000266.4:c.113G>A