Canonical Allele Identifier: PA2827921226
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 936508
ClinVar RCV Id: RCV003591847 RCV002451432 RCV003656465
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Thr38Ile
CA352158800
NM_001354701.2:c.113C>T