Canonical Allele Identifier: PA2827924012
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 923347

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Glu1883Gln
CA352140265
NM_001354701.2:c.5647G>C