Allele Registry

Canonical Allele Identifier: PA107951

Gene: NEFL HGNC NCBI

ClinVar RCV:

RCV000057133

RCV001854171

ClinVar Variation:

66690

HGVS (amino-acid)	Matching Registered Transcripts
NP_006149.2:p.Glu90Lys	CA217539 NM_006158.5:c.268G>A