Canonical Allele Identifier: PA2826291111
Gene: CNTN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3146759
ClinVar RCV Id: RCV004442129
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193885.1:p.Glu371Asp
CA351447865
NM_001206956.2:c.1113A>C
CA351447868
NM_001206956.2:c.1113A>T