Canonical Allele Identifier: PA101228
Gene: NDP HGNC NCBI

Linked Data

ClinVar Variation Id: 10688
ClinVar RCV Id: RCV000011434 RCV000484893 RCV003334376
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000257.1:p.Arg121Trp
CA255477
NM_000266.4:c.361C>T