Canonical Allele Identifier: PA330249
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67989

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Asp1789Gly
CA019174
NM_000335.5:c.5366A>G