Canonical Allele Identifier: PA101644
Gene: NDP HGNC NCBI

Linked Data

ClinVar Variation Id: 10680
ClinVar RCV Id: RCV000011426 RCV003313916
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000257.1:p.Ser75Cys
CA255467
NM_000266.4:c.224C>G