Canonical Allele Identifier: PA2499230622
Gene: NDP HGNC NCBI

Linked Data

ClinVar Variation Id: 1219131
ClinVar RCV Id: RCV001594327
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000257.1:p.Cys110Phe
CA413007398
NM_000266.4:c.329G>T