Canonical Allele Identifier: PA2825940691
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67672

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Arg535Gln
CA015071
NM_001160160.2:c.1604G>A