Canonical Allele Identifier: PA2825942542
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67981
ClinVar RCV Id: RCV000058767
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Leu1739Val
CA019110
NM_001160160.2:c.5215C>G