Canonical Allele Identifier: PA2825493477
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2091499
ClinVar RCV Id: RCV003658552

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Glu553Lys
CA352146931
NM_001099405.2:c.1657G>A