Allele Registry

Canonical Allele Identifier: PA101615

Gene: NDP HGNC NCBI

ClinVar RCV:

RCV000440494

RCV005133559

ClinVar Variation:

378238

3653663

HGVS (amino-acid)	Matching Registered Transcripts
NP_000257.1:p.Phe89Leu	CA16608479 NM_000266.4:c.267C>G CA413007615 NM_000266.4:c.267C>A CA413007621 NM_000266.4:c.265T>C