Canonical Allele Identifier: PA307546
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201496
ClinVar RCV Id: RCV000183038 RCV001842917
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Val1181Leu
CA017238
NM_001099404.2:c.3541G>T
CA352138243
NM_001099404.2:c.3541G>C