Canonical Allele Identifier: PA100284
Gene: CTH HGNC NCBI

Linked Data

ClinVar Variation Id: 2939
ClinVar RCV Id: RCV000003073 RCV000727631
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001893.2:p.Thr67Ile
CA115889
NM_001902.6:c.200C>T