Canonical Allele Identifier: PA2825942249
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1378047
ClinVar RCV Id: RCV003772645
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Glu1554Asp
CA352143889
NM_001160160.2:c.4662G>T
CA352143890
NM_001160160.2:c.4662G>C