Allele Registry

Canonical Allele Identifier: PA101413

Gene: NDP HGNC NCBI

ClinVar RCV:

RCV000011429

ClinVar Variation:

10683

HGVS (amino-acid)	Matching Registered Transcripts
NP_000257.1:p.Cys96Tyr	CA255470 NM_000266.4:c.287G>A