Allele Registry

Canonical Allele Identifier: PA658679838

Gene: NEFL HGNC NCBI

ClinVar Allele:

441227

ClinVar RCV:

RCV000516482

RCV000809657

RCV001027486

RCV001584230

RCV002420299

RCV002490884

ClinVar Variation:

447763

HGVS (amino-acid)	Matching Registered Transcripts
NP_006149.2:p.Tyr265Asp	CA370621618 NM_006158.5:c.793T>G