Canonical Allele Identifier: PA2580108379
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 2267439
ClinVar RCV Id: RCV002804091
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Gly1118Ser
CA400620689
NM_000334.4:c.3352G>A