Canonical Allele Identifier: PA645453667
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 243042
ClinVar RCV Id: RCV000235032 RCV001056500 RCV002512068 RCV003227471
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Arg1454Trp
CA10584065
NM_000334.4:c.4360C>T