Canonical Allele Identifier: PA2825492663
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68053

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Gly292Ser
CA019893
NM_001099405.2:c.874G>A