Canonical Allele Identifier: PA2825490852
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1057952
ClinVar RCV Id: RCV001367028
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Ser1718Arg
CA064180
NM_001099404.2:c.5154C>A
CA352142161
NM_001099404.2:c.5154C>G
CA352142170
NM_001099404.2:c.5152A>C