Canonical Allele Identifier: PA2825942427
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67955
ClinVar RCV Id: RCV000058740
ClinVar Variation Id: 2857136
ClinVar RCV Id: RCV003696758
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Gln1673His
CA018890
NM_001160160.2:c.5019G>C
CA352142300
NM_001160160.2:c.5019G>T