Canonical Allele Identifier: PA645490438
Gene: NEFL HGNC NCBI

Linked Data

ClinVar Variation Id: 412304

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006149.2:p.Gln274Arg
CA4681434
NM_006158.5:c.821A>G