Canonical Allele Identifier: PA2825165886
Gene: L1CAM HGNC NCBI

Linked Data

ClinVar Variation Id: 1307929
ClinVar RCV Id: RCV001772784
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000416.1:p.Gly257Arg
CA415133132
NM_000425.5:c.769G>C
CA415133135
NM_000425.5:c.769G>A