Canonical Allele Identifier: PA2825492145
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67798
ClinVar RCV Id: RCV000058572

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Ser115Gly
CA017168
NM_001099405.2:c.343A>G