Canonical Allele Identifier: PA2825130581
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 639665
ClinVar RCV Id: RCV003540869

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Glu1061Asp
CA061337
NM_000335.5:c.3183A>C
CA352139126
NM_000335.5:c.3183A>T