Canonical Allele Identifier: PA107998
Gene: NEFL HGNC NCBI

Linked Data

ClinVar Variation Id: 66689
ClinVar RCV Id: RCV000057132 RCV001235472 RCV003278661
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006149.2:p.Pro8Leu
CA217537
NM_006158.5:c.23C>T