Canonical Allele Identifier: PA2827491503
Gene: CNTN4 HGNC NCBI
ClinVar RCV:
RCV000329641
ClinVar Variation:
283737
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337024.1:p.Asn178Asp
CA2227072
NM_001350095.2:c.532A>G