Canonical Allele Identifier: PA107920
Gene: NEFL HGNC NCBI

Linked Data

ClinVar Variation Id: 14028
ClinVar RCV Id: RCV000015072 RCV000057151
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006149.2:p.Gln332Pro
CA217588
NM_006158.5:c.995A>C