Canonical Allele Identifier: PA101401
Gene: NDP HGNC NCBI

Linked Data

ClinVar Variation Id: 10696
ClinVar RCV Id: RCV000011442
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000257.1:p.Cys96Trp
CA255483
NM_000266.4:c.288C>G