Canonical Allele Identifier: PA2827921243
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1430634

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Glu50Gly
CA352158516
NM_001354701.2:c.149A>G