Canonical Allele Identifier: PA2825132012
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1189625
ClinVar RCV Id: RCV001550047
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Gly1638Glu
CA352142972
NM_000335.5:c.4913G>A