Allele Registry

Canonical Allele Identifier: PA107959

Gene: NEFL HGNC NCBI

ClinVar RCV:

RCV000143807

RCV001173041

ClinVar Variation:

155737

HGVS (amino-acid)	Matching Registered Transcripts
NP_006149.2:p.Leu336Pro	CA233074 NM_006158.5:c.1007T>C