Canonical Allele Identifier: PA2825942435
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9383

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Ser1677Leu
CA018910
NM_001160160.2:c.5030C>T