Canonical Allele Identifier: PA916072269
Gene: L1CAM HGNC NCBI

Linked Data

ClinVar Variation Id: 9991

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_076493.1:p.Arg184Gln
CA254959
NM_024003.3:c.551G>A