Canonical Allele Identifier: PA217564
Gene: NEFL HGNC NCBI

Linked Data

ClinVar Variation Id: 66695
ClinVar RCV Id: RCV000057142 RCV000507003 RCV001081393 RCV001160882 RCV001173051 RCV002362689 RCV003925018
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006149.2:p.Ile213Met
CA217562
NM_006158.5:c.639C>G