Canonical Allele Identifier: PA2825943376
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2774490

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Asn288Ser
CA065779
NM_001160161.2:c.863A>G