Canonical Allele Identifier: PA2741926827
Gene: NEFL HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006149.2:p.Tyr389Ser
CA370620765
NM_006158.5:c.1166A>C