Canonical Allele Identifier: PA2827923075
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1382658
ClinVar RCV Id: RCV003657389

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Leu1290Val
CA352148232
NM_001354701.2:c.3868C>G