Canonical Allele Identifier: PA2825493414
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67672

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Arg535Gln
CA015071
NM_001099405.2:c.1604G>A