Canonical Allele Identifier: PA2827419468
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_001334923.1:p.Asn1017Ser
CA174124
NM_001347994.1:c.3050A>G