Canonical Allele Identifier: PA206515
Gene: CNTN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 210738
ClinVar RCV Id: RCV000193196
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001834.2:p.Tyr91His
CA206514
NM_001843.4:c.271T>C