Canonical Allele Identifier: PA891855384
Gene: NEFL HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006149.2:p.Glu385Val
CA370620789
NM_006158.5:c.1154A>T