Canonical Allele Identifier: PA2827923607
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9369

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Arg1625His
CA018760
NM_001354701.2:c.4874G>A