Canonical Allele Identifier: PA2741976302
Gene: NEFH HGNC NCBI

Linked Data

ClinVar Variation Id: 2957103
ClinVar RCV Id: RCV003818790
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066554.2:p.Ala41Val
CA411121461
NM_021076.4:c.122C>T