Allele Registry

Canonical Allele Identifier: PA101695

Gene: NDP HGNC NCBI

ClinVar RCV:

RCV000011443

ClinVar Variation:

10697

HGVS (amino-acid)	Matching Registered Transcripts
NP_000257.1:p.Val45Glu	CA255484 NM_000266.4:c.134T>A