Canonical Allele Identifier: PA101300
Gene: NDP HGNC NCBI
ClinVar RCV:
RCV000011440
ClinVar Variation:
10694
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000257.1:p.Cys110Gly
CA255481
NM_000266.4:c.328T>G