Canonical Allele Identifier: PA2825497504
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 75052

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Arg1911Cys
CA064797
NM_001099405.2:c.5731C>T