Canonical Allele Identifier: PA101603
Gene: NDP HGNC NCBI

Linked Data

ClinVar Variation Id: 1303053
ClinVar RCV Id: RCV001756552
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000257.1:p.Lys58Asn
CA413008938
NM_000266.4:c.174G>T
CA413008939
NM_000266.4:c.174G>C