Canonical Allele Identifier: PA2830047211
Gene: WWC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2369766
ClinVar RCV Id: RCV004207468
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079225.5:p.Arg1082Leu
CA3150308
NM_024949.6:c.3245G>T