Canonical Allele Identifier: PA107765
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67812

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Glu1231Lys
CA017410
NM_198056.3:c.3691G>A