Canonical Allele Identifier: PA2826787942
Gene: NWD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 782639
ClinVar RCV Id: RCV000964056
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001277284.1:p.Val588Phe
CA9281961
NM_001290355.3:c.1762G>T