Canonical Allele Identifier: PA2825943109
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1719781
ClinVar RCV Id: RCV002305023

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Lys91Met
CA352157704
NM_001160161.2:c.272A>T