Canonical Allele Identifier: PA2826291135
Gene: CNTN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2485833
ClinVar RCV Id: RCV004277139
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193885.1:p.Tyr611Phe
CA2227869
NM_001206956.2:c.1832A>T