Allele Registry

Canonical Allele Identifier: PA217572

Gene: NEFL HGNC NCBI

ClinVar RCV:

RCV000034139

RCV000057145

ClinVar Variation:

41239

HGVS (amino-acid)	Matching Registered Transcripts
NP_006149.2:p.Pro22Arg	CA217570 NM_006158.5:c.65C>G