Allele Registry

Canonical Allele Identifier: PA645502614

Gene: NDP HGNC NCBI

ClinVar RCV:

RCV000415329

ClinVar Variation:

374014

HGVS (amino-acid)	Matching Registered Transcripts
NP_000257.1:p.Ala105Val	CA16043592 NM_000266.4:c.314C>T