Canonical Allele Identifier: PA2825940738
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1306695
ClinVar RCV Id: RCV001770875
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Val563Leu
CA352146717
NM_001160160.2:c.1687G>T
CA352146720
NM_001160160.2:c.1687G>C