Canonical Allele Identifier: PA645502614
Gene: NDP HGNC NCBI

Linked Data

ClinVar Variation Id: 374014
ClinVar RCV Id: RCV000415329
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000257.1:p.Ala105Val
CA16043592
NM_000266.4:c.314C>T