Canonical Allele Identifier: PA101523
Gene: NDP HGNC NCBI
ClinVar RCV:
RCV000011435
ClinVar Variation:
10689
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000257.1:p.Leu13Arg
CA255478
NM_000266.4:c.38T>G