Canonical Allele Identifier: PA2825537444
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1430634

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Glu50Gly
CA352158516
NM_001099404.2:c.149A>G