Canonical Allele Identifier: PA645490446
Gene: NEFL HGNC NCBI

Linked Data

ClinVar Variation Id: 234913
ClinVar RCV Id: RCV000762503 RCV000535984 RCV000764773
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006149.2:p.Leu329Pro
CA10577361
NM_006158.5:c.986T>C