Canonical Allele Identifier: PA107937
Gene: NEFL HGNC NCBI

Linked Data

ClinVar Variation Id: 66671
ClinVar RCV Id: RCV000057113 RCV000534161 RCV000585797 RCV001174356
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006149.2:p.Glu396Lys
CA217487
NM_006158.5:c.1186G>A