Canonical Allele Identifier: PA915960971
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 805396
ClinVar RCV Id: RCV000992902 RCV001858760
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Thr1684Ile
CA8708846
NM_000334.4:c.5051C>T