Canonical Allele Identifier: PA2573062131
Gene: NDP HGNC NCBI

Linked Data

ClinVar Variation Id: 1339792
ClinVar RCV Id: RCV001825175
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000257.1:p.Leu62Pro
CA413008056
NM_000266.4:c.185T>C