Canonical Allele Identifier: PA2825942759
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 919315

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Met1873Val
CA72937834
NM_001160160.2:c.5617A>G