Canonical Allele Identifier: PA2826291129
Gene: CNTN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3146764
ClinVar RCV Id: RCV004442134
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193885.1:p.Gly577Arg
CA2227821
NM_001206956.2:c.1729G>A
CA351451395
NM_001206956.2:c.1729G>C