Canonical Allele Identifier: PA645490453
Gene: NEFL HGNC NCBI

Linked Data

ClinVar Variation Id: 245748
ClinVar RCV Id: RCV000640659 RCV000857196 RCV001711645
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006149.2:p.Leu393Phe
CA10584291
NM_006158.5:c.1179G>C
CA370620722
NM_006158.5:c.1179G>T