Canonical Allele Identifier: PA2580109318
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 2081754
ClinVar RCV Id: RCV002995589
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Glu1649Lys
CA400614486
NM_000334.4:c.4945G>A