Canonical Allele Identifier: PA2825496824
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9383

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Ser1692Leu
CA018910
NM_001099405.2:c.5075C>T