Canonical Allele Identifier: PA915955244
Gene: NWD1 HGNC NCBI
ClinVar RCV:
RCV000964056
ClinVar Variation:
782639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001007526.3:p.Val723Phe
CA9281961
NM_001007525.5:c.2167G>T