Canonical Allele Identifier: PA2825492027
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3229481
ClinVar RCV Id: RCV004525059

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Pro79Ser
CA060252
NM_001099405.2:c.235C>T