Canonical Allele Identifier: PA2825942595
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 628960

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Asp1769Glu
CA352141178
NM_001160160.2:c.5307C>G
CA352141179
NM_001160160.2:c.5307C>A