Allele Registry

Canonical Allele Identifier: PA355610

Gene: NEFL HGNC NCBI

ClinVar Allele:

221759

ClinVar RCV:

RCV000205038

ClinVar Variation:

219429

HGVS (amino-acid)	Matching Registered Transcripts
NP_006149.2:p.Pro22His	CA349198 NM_006158.5:c.65C>A