Canonical Allele Identifier: PA2741815131
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 2648092
ClinVar RCV Id: RCV003428406
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Lys566Gln
CA400633576
NM_000334.4:c.1696A>C