Canonical Allele Identifier: PA307824
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67974

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Val1763Met
CA019062
NM_001099404.2:c.5287G>A