Canonical Allele Identifier: PA2825128203
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1430634

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Glu50Gly
CA352158516
NM_000335.5:c.149A>G