Canonical Allele Identifier: PA2830047212
Gene: WWC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2375939
ClinVar RCV Id: RCV004213172
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079225.5:p.Arg1082Cys
CA3150307
NM_024949.6:c.3244C>T