Allele Registry

Canonical Allele Identifier: PA2573062132

Gene: NDP HGNC NCBI

ClinVar Allele:

1330696

ClinVar RCV:

RCV001824259

ClinVar Variation:

1339550

HGVS (amino-acid)	Matching Registered Transcripts
NP_000257.1:p.Phe81Ser	CA413007757 NM_000266.4:c.242T>C