Canonical Allele Identifier: PA2499303299
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1013702
ClinVar RCV Id: RCV003770639

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Thr1367Pro
CA352146994
NM_198056.3:c.4099A>C