Canonical Allele Identifier: PA107914
Gene: NEFL HGNC NCBI

Linked Data

ClinVar Variation Id: 41236
ClinVar RCV Id: RCV000034136 RCV000057136 RCV000585792 RCV000554079 RCV000857201 RCV001027680 RCV001843465
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006149.2:p.Asn98Ser
CA217547
NM_006158.5:c.293A>G