Canonical Allele Identifier: PA2827922932
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201497

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Arg1192Trp
CA017280
NM_001354701.2:c.3574C>T