Canonical Allele Identifier: PA307137
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68004

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Arg190Gly
CA019420
NM_000335.5:c.568C>G