Canonical Allele Identifier: PA2825490525
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3073613
ClinVar RCV Id: RCV004016619

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Val1599Leu
CA352143606
NM_001099404.2:c.4795G>C