Canonical Allele Identifier: PA2825497355
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 965989
ClinVar RCV Id: RCV002290656

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Glu1859del
CA352140560
NM_001099405.2:c.5575G>T
CA352140574
NM_001099405.2:c.5572G>T
CA1358556507
NM_001099405.2:c.5575_5577del