Canonical Allele Identifier: PA2825940987
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1299964
ClinVar RCV Id: RCV001730414

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Phe733Leu
CA059897
NM_001160160.2:c.2199C>G
CA72932536
NM_001160160.2:c.2199C>A
CA352144561
NM_001160160.2:c.2197T>C