Canonical Allele Identifier: PA107992
Gene: NEFL HGNC NCBI

Linked Data

ClinVar Variation Id: 66687
ClinVar RCV Id: RCV000057130 RCV001174358
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006149.2:p.Pro8Gln
CA217534
NM_006158.5:c.23C>A