Canonical Allele Identifier: PA915960980
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 805397
ClinVar RCV Id: RCV000992903
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Thr1721Ile
CA400613697
NM_000334.4:c.5162C>T