Canonical Allele Identifier: PA2825490460
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 830371
ClinVar RCV Id: RCV001030819
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Phe1571Leu
CA352143783
NM_001099404.2:c.4713C>G
CA352143784
NM_001099404.2:c.4713C>A
CA352143788
NM_001099404.2:c.4711T>C