Canonical Allele Identifier: PA658679838
Gene: NEFL HGNC NCBI

Linked Data

ClinVar Variation Id: 447763
ClinVar RCV Id: RCV000516482 RCV001027486 RCV001584230 RCV002490884 RCV000809657 RCV002420299
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006149.2:p.Tyr265Asp
CA370621618
NM_006158.5:c.793T>G