Canonical Allele Identifier: PA2827923000
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67815

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Lys1235Arg
CA017434
NM_001354701.2:c.3704A>G