Canonical Allele Identifier: PA2825491547
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2797141
ClinVar RCV Id: RCV003671042

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Glu1945Asp
CA352139771
NM_001099404.2:c.5835G>T
CA352139772
NM_001099404.2:c.5835G>C