Canonical Allele Identifier: PA2825496038
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67866
ClinVar RCV Id: RCV000058645 RCV003330080 RCV003591671
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Val1405Met
CA017946
NM_001099405.2:c.4213G>A