Canonical Allele Identifier: PA2827922988
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 463328
ClinVar RCV Id: RCV003654430

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Glu1229Lys
CA062201
NM_001354701.2:c.3685G>A