Canonical Allele Identifier: PA891865992
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_001268885.1:p.Arg2603Leu
CA174790
NM_001281956.2:c.7808G>T