Canonical Allele Identifier: PA2580444034
Gene: NEFH HGNC NCBI

Linked Data

ClinVar Variation Id: 1777018
ClinVar RCV Id: RCV002403535 RCV003774426
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066554.2:p.Val55Leu
CA411121699
NM_021076.4:c.163G>C
CA411121701
NM_021076.4:c.163G>T