Canonical Allele Identifier: PA2825495565
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67819

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Tyr1241Ser
CA017466
NM_001099405.2:c.3722A>C