Allele Registry

Canonical Allele Identifier: PA101552

Gene: NDP HGNC NCBI

ClinVar RCV:

RCV000011436

ClinVar Variation:

10690

HGVS (amino-acid)	Matching Registered Transcripts
NP_000257.1:p.Leu61Phe	CA255479 NM_000266.4:c.181C>T