Canonical Allele Identifier: PA2573166354
Gene: NDP HGNC NCBI

Linked Data

ClinVar Variation Id: 1678208
ClinVar RCV Id: RCV002224799
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000257.1:p.Cys93Arg
CA413007572
NM_000266.4:c.277T>C