Canonical Allele Identifier: PA2825942919
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 859529
ClinVar RCV Id: RCV003656394

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Glu1966Asp
CA352139153
NM_001160160.2:c.5898A>T
CA352139157
NM_001160160.2:c.5898A>C