Canonical Allele Identifier: PA645502623
Gene: NDP HGNC NCBI

Linked Data

ClinVar Variation Id: 377374
ClinVar RCV Id: RCV000441399

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000257.1:p.Glu129Lys
CA10391402
NM_000266.4:c.385G>A