Canonical Allele Identifier: PA915980252
Gene: CPLX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 736367
ClinVar RCV Id: RCV000912006
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006642.1:p.Pro103Leu
CA2796910
NM_006651.4:c.308C>T