Allele Registry

Canonical Allele Identifier: PA101716

Gene: NDP HGNC NCBI

ClinVar RCV:

RCV000011427

ClinVar Variation:

10681

HGVS (amino-acid)	Matching Registered Transcripts
NP_000257.1:p.Val60Glu	CA255468 NM_000266.4:c.179T>A