Canonical Allele Identifier: PA2825490742
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 958530
ClinVar RCV Id: RCV003656685
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Phe1669Leu
CA72938220
NM_001099404.2:c.5007C>A
CA352142782
NM_001099404.2:c.5007C>G
CA352142793
NM_001099404.2:c.5005T>C