Canonical Allele Identifier: PA645490341
Gene: NEFL HGNC NCBI

Linked Data

ClinVar Variation Id: 372433
ClinVar RCV Id: RCV000413716 RCV001071579
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006149.2:p.Asn98Lys
CA16042636
NM_006158.5:c.294T>G
CA370622888
NM_006158.5:c.294T>A