Canonical Allele Identifier: PA2825941756
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2725883
ClinVar RCV Id: RCV003554729

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Thr1233Ser
CA352149372
NM_001160160.2:c.3698C>G
CA352149391
NM_001160160.2:c.3697A>T