Canonical Allele Identifier: PA093083
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 143201
ClinVar RCV Id: RCV000132737 RCV000254971 RCV000797599 RCV002305449
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Arg1135His
CA345720
NM_000334.4:c.3404G>A