Canonical Allele Identifier: PA254776
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9382

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Tyr1795_Glu1796insAsp
CA025554
NM_198056.3:c.5385_5387dup