Allele Registry

Canonical Allele Identifier: PA107914

Gene: NEFL HGNC NCBI

ClinVar RCV:

RCV000034136

RCV000057136

RCV000554079

RCV000585792

RCV000857201

RCV001027680

RCV001843465

ClinVar Variation:

41236

HGVS (amino-acid)	Matching Registered Transcripts
NP_006149.2:p.Asn98Ser	CA217547 NM_006158.5:c.293A>G