Canonical Allele Identifier: PA2580444045
Gene: NEFH HGNC NCBI

Linked Data

ClinVar Variation Id: 1795179
ClinVar RCV Id: RCV002431278 RCV003730226
ClinVar Variation Id: 2976160
ClinVar RCV Id: RCV003836310
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066554.2:p.Val91Leu
CA411122332
NM_021076.4:c.271G>C
CA411122335
NM_021076.4:c.271G>T