Canonical Allele Identifier: PA101442
Gene: NDP HGNC NCBI

Linked Data

ClinVar Variation Id: 1373871
ClinVar RCV Id: RCV001882960
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000257.1:p.Gly67Glu
CA413007974
NM_000266.4:c.200G>A