Canonical Allele Identifier: PA2580335058
Gene: NEFL HGNC NCBI

Linked Data

ClinVar Variation Id: 2260002
ClinVar RCV Id: RCV002783311 RCV003130875
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006149.2:p.Val47Leu
CA4681547
NM_006158.5:c.139G>T
CA370623904
NM_006158.5:c.139G>C