Canonical Allele Identifier: PA2826370763
Gene: CNTN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 423311
ClinVar RCV Id: RCV000481172 RCV001044442
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001242993.1:p.Met93Thr
CA6516571
NM_001256064.2:c.278T>C