Canonical Allele Identifier: PA2825491738
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 345111
ClinVar RCV Id: RCV000287762 RCV000291687 RCV000322026 RCV000346616 RCV000351997 RCV000376753 RCV000403611
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Asp2011Glu
CA10618690
NM_001099404.2:c.6033C>A
CA352139019
NM_001099404.2:c.6033C>G