Canonical Allele Identifier: PA2825490800
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 427788
ClinVar RCV Id: RCV000492065 RCV003541189
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Met1701Ile
CA064131
NM_001099404.2:c.5103G>T
CA352142354
NM_001099404.2:c.5103G>C
CA352142355
NM_001099404.2:c.5103G>A