Canonical Allele Identifier: PA2825132427
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 628960

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Asp1801Glu
CA352141178
NM_000335.5:c.5403C>G
CA352141179
NM_000335.5:c.5403C>A