Canonical Allele Identifier: PA2827923115
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 216840

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Arg1315Leu
CA062580
NM_001354701.2:c.3944G>T