Canonical Allele Identifier: PA2573166353
Gene: NDP HGNC NCBI

Linked Data

ClinVar Variation Id: 1474690
ClinVar RCV Id: RCV002007685 RCV002441134
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000257.1:p.Ser92Thr
CA10391408
NM_000266.4:c.274T>A