Canonical Allele Identifier: PA107951
Gene: NEFL HGNC NCBI

Linked Data

ClinVar Variation Id: 66690
ClinVar RCV Id: RCV000057133 RCV001854171
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006149.2:p.Glu90Lys
CA217539
NM_006158.5:c.268G>A