Canonical Allele Identifier: PA2580348119
Gene: CPLX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2277799
ClinVar RCV Id: RCV002844212
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006642.1:p.Gly92Trp
CA355921609
NM_006651.4:c.274G>T