Canonical Allele Identifier: PA2825495857
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67844

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Pro1332Leu
CA017721
NM_001099405.2:c.3995C>T