Canonical Allele Identifier: PA2825497067
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 919539
ClinVar RCV Id: RCV001842702

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Glu1766Asp
CA352141338
NM_001099405.2:c.5298G>T
CA352141339
NM_001099405.2:c.5298G>C