Canonical Allele Identifier: PA093269
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 5903
ClinVar RCV Id: RCV000006264 RCV000006265 RCV000479620 RCV000690377 RCV002267601
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Gly1306Val
CA117840
NM_000334.4:c.3917G>T