Canonical Allele Identifier: PA307351
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201467

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Ala665Ser
CA015703
NM_198056.3:c.1993G>T