Canonical Allele Identifier: PA2825537730
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2143286
ClinVar RCV Id: RCV003542395

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Asp305Glu
CA352150352
NM_001099404.2:c.915C>G
CA352150353
NM_001099404.2:c.915C>A