Canonical Allele Identifier: PA101486
Gene: NDP HGNC NCBI

Linked Data

ClinVar Variation Id: 2737210
ClinVar RCV Id: RCV003560232
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000257.1:p.Ile123Asn
CA413007306
NM_000266.4:c.368T>A