Canonical Allele Identifier: PA2827491715
Gene: CNTN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2600857
ClinVar RCV Id: RCV004349783

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337024.1:p.Asp965Asn
CA2227885
NM_001350095.2:c.2893G>A