Canonical Allele Identifier: PA2825497086
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67989

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Asp1772Gly
CA019174
NM_001099405.2:c.5315A>G