Canonical Allele Identifier: PA307138
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68004

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Arg190Gly
CA019420
NM_001099404.2:c.568C>G