Canonical Allele Identifier: PA891845964
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 586520
ClinVar RCV Id: RCV000713113 RCV001053863
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Ala1474Thr
CA8708964
NM_000334.4:c.4420G>A