Canonical Allele Identifier: PA915958701
Gene: NDP HGNC NCBI

Linked Data

ClinVar Variation Id: 812352
ClinVar RCV Id: RCV001003091 RCV001306511 RCV001375287 RCV004526061
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000257.1:p.Arg90His
CA10391409
NM_000266.4:c.269G>A