Canonical Allele Identifier: PA2825497300
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1005584

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Ile1835Leu
CA352140853
NM_001099405.2:c.5503A>C