Allele Registry

Canonical Allele Identifier: PA101456

Gene: NDP HGNC NCBI

ClinVar RCV:

RCV000011437

RCV000520034

ClinVar Variation:

10691

HGVS (amino-acid)	Matching Registered Transcripts
NP_000257.1:p.His42Arg	CA121146 NM_000266.4:c.125A>G