Canonical Allele Identifier: PA1139678673
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 840491
ClinVar RCV Id: RCV001042494 RCV003405231
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Glu1622Lys
CA8708891
NM_000334.4:c.4864G>A