Canonical Allele Identifier: PA2826787976
Gene: NWD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 161488
ClinVar RCV Id: RCV000149022
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001277284.1:p.Asn1088Ser
CA174124
NM_001290355.3:c.3263A>G