Canonical Allele Identifier: PA2825860082
Gene: L1CAM HGNC NCBI

Linked Data

ClinVar Variation Id: 392922
ClinVar RCV Id: RCV000433806

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137435.1:p.Phe776Leu
CA16608779
NM_001143963.2:c.2328C>G
CA415120205
NM_001143963.2:c.2328C>A
CA415120221
NM_001143963.2:c.2326T>C