Canonical Allele Identifier: PA2741813899
Gene: NDP HGNC NCBI

Linked Data

ClinVar Variation Id: 3001312
ClinVar RCV Id: RCV003852455
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000257.1:p.Leu116Phe
CA413007349
NM_000266.4:c.346C>T