Canonical Allele Identifier: PA645504644
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 423924

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Arg693Cys
CA059716
NM_198056.3:c.2077C>T