Canonical Allele Identifier: PA2580109603
Gene: NDP HGNC NCBI

Linked Data

ClinVar Variation Id: 2169642
ClinVar RCV Id: RCV003093216
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000257.1:p.Lys58Arg
CA413008941
NM_000266.4:c.173A>G