Canonical Allele Identifier: PA2830380535
Gene: CNTN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3146764
ClinVar RCV Id: RCV004442134
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_783200.1:p.Gly906Arg
CA2227821
NM_175607.3:c.2716G>A
CA351451395
NM_175607.3:c.2716G>C