Canonical Allele Identifier: PA308035
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67739

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Thr843Ala
CA016243
NM_198056.3:c.2527A>G