Canonical Allele Identifier: PA2825940784
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1485298
ClinVar RCV Id: RCV003657590
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Val595Leu
CA352146177
NM_001160160.2:c.1783G>T
CA352146178
NM_001160160.2:c.1783G>C