Canonical Allele Identifier: PA2825537381
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 928310

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Pro7Ser
CA72951858
NM_001099404.2:c.19C>T