Canonical Allele Identifier: PA2827923981
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1035159

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Ala1863Val
CA352140486
NM_001354701.2:c.5588C>T