Canonical Allele Identifier: PA265653
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67917

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Phe1570Cys
CA018496
NM_000335.5:c.4709T>G