Canonical Allele Identifier: PA2825943101
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2893345

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Pro85Ser
CA060576
NM_001160161.2:c.253C>T