Allele Registry

Canonical Allele Identifier: PA891855357

Gene: NEFL HGNC NCBI

ClinVar RCV:

RCV000688624

RCV002289963

ClinVar Variation:

568307

HGVS (amino-acid)	Matching Registered Transcripts
NP_006149.2:p.Glu140Lys	CA4681508 NM_006158.5:c.418G>A