Canonical Allele Identifier: PA2580109598
Gene: NDP HGNC NCBI

Linked Data

ClinVar Variation Id: 2169643
ClinVar RCV Id: RCV003084931
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000257.1:p.Cys55Tyr
CA413008963
NM_000266.4:c.164G>A