Canonical Allele Identifier: PA101456
Gene: NDP HGNC NCBI

Linked Data

ClinVar Variation Id: 10691
ClinVar RCV Id: RCV000011437 RCV000520034
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000257.1:p.His42Arg
CA121146
NM_000266.4:c.125A>G