Allele Registry

Canonical Allele Identifier: PA101228

Gene: NDP HGNC NCBI

ClinVar RCV:

RCV000011434

RCV000484893

RCV003334376

ClinVar Variation:

10688

HGVS (amino-acid)	Matching Registered Transcripts
NP_000257.1:p.Arg121Trp	CA255477 NM_000266.4:c.361C>T