Canonical Allele Identifier: PA101422
Gene: NDP HGNC NCBI

Linked Data

ClinVar Variation Id: 2138556
ClinVar RCV Id: RCV003041441
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000257.1:p.Gly112Glu
CA413007379
NM_000266.4:c.335G>A