Canonical Allele Identifier: PA2827921466
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1509648
ClinVar RCV Id: RCV003773407
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Trp195Arg
CA352153586
NM_001354701.2:c.583T>A
CA352153588
NM_001354701.2:c.583T>C