Canonical Allele Identifier: PA2825491357
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3071902
ClinVar RCV Id: RCV004011932

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Met1868Thr
CA352140673
NM_001099404.2:c.5603T>C