Canonical Allele Identifier: PA2825945727
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 965989
ClinVar RCV Id: RCV002290656

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Glu1823del
CA352140560
NM_001160161.2:c.5467G>T
CA352140574
NM_001160161.2:c.5464G>T
CA1358556507
NM_001160161.2:c.5467_5469del