Allele Registry

Canonical Allele Identifier: PA107969

Gene: NEFL HGNC NCBI

ClinVar RCV:

RCV000015073

RCV000057144

RCV000194357

RCV000414916

RCV000415401

RCV001196666

RCV002362585

ClinVar Variation:

14029

HGVS (amino-acid)	Matching Registered Transcripts
NP_006149.2:p.Pro22Ser	CA217568 NM_006158.5:c.64C>T