Canonical Allele Identifier: PA265424
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67855
ClinVar RCV Id: RCV000058634

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Ile1350Thr
CA017817
NM_001099404.2:c.4049T>C