Canonical Allele Identifier: PA2827923976
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 965989
ClinVar RCV Id: RCV002290656

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Glu1858del
CA352140560
NM_001354701.2:c.5572G>T
CA352140574
NM_001354701.2:c.5569G>T
CA1358556507
NM_001354701.2:c.5572_5574del