Canonical Allele Identifier: PA2825942061
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2875975
ClinVar RCV Id: RCV003707531

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Gly1432Arg
CA72943607
NM_001160160.2:c.4294G>A
CA352145548
NM_001160160.2:c.4294G>C