Canonical Allele Identifier: PA265719
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67940

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Gly1642Glu
CA018747
NM_198056.3:c.4925G>A