Canonical Allele Identifier: PA2825497419
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 219835

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Val1885Leu
CA348136
NM_001099405.2:c.5653G>T
CA352140249
NM_001099405.2:c.5653G>C