Canonical Allele Identifier: PA2825129915
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 855794

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Pro773Arg
CA352143437
NM_000335.5:c.2318C>G