Canonical Allele Identifier: PA2499230620
Gene: NDP HGNC NCBI

Linked Data

ClinVar Variation Id: 1299928
ClinVar RCV Id: RCV001730365
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000257.1:p.Ser80Leu
CA413007766
NM_000266.4:c.239C>T