Canonical Allele Identifier: PA2825491265
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2810685
ClinVar RCV Id: RCV003682543
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Ser1844Arg
CA352140909
NM_001099404.2:c.5532T>G
CA352140910
NM_001099404.2:c.5532T>A
CA352140915
NM_001099404.2:c.5530A>C