Canonical Allele Identifier: PA174125
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_001007526.3:p.Asn1223Ser
CA174124
NM_001007525.5:c.3668A>G