Canonical Allele Identifier: PA107969
Gene: NEFL HGNC NCBI

Linked Data

ClinVar Variation Id: 14029
ClinVar RCV Id: RCV000015073 RCV000057144 RCV000194357 RCV000415401 RCV000414916 RCV001196666 RCV002362585
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006149.2:p.Pro22Ser
CA217568
NM_006158.5:c.64C>T