Canonical Allele Identifier: PA2827922513
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2006013

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Leu935Val
CA352140756
NM_001354701.2:c.2803C>G