Canonical Allele Identifier: PA2825942791
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9381

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Ala1891Thr
CA019460
NM_001160160.2:c.5671G>A