Canonical Allele Identifier: PA107875
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9395

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Gly1408Arg
CA017985
NM_198056.3:c.4222G>A
CA352146220
NM_198056.3:c.4222G>C