Canonical Allele Identifier: PA645378723
Gene: CNTN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 421523
ClinVar RCV Id: RCV000487172 RCV001205215
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001834.2:p.Gly882Arg
CA6517196
NM_001843.4:c.2644G>A
CA384587644
NM_001843.4:c.2644G>C