Allele Registry

Canonical Allele Identifier: PA101219

Gene: NDP HGNC NCBI

ClinVar RCV:

RCV000011441

ClinVar Variation:

10695

HGVS (amino-acid)	Matching Registered Transcripts
NP_000257.1:p.Arg121Leu	CA255482 NM_000266.4:c.362G>T