Canonical Allele Identifier: PA174791
Gene: CSMD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 161791
ClinVar RCV Id: RCV000149327
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443128.2:p.Arg2605Leu
CA174790
NM_052896.5:c.7814G>T