Canonical Allele Identifier: PA2825497097
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 998587
ClinVar RCV Id: RCV003770481

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Met1775Ile
CA352141245
NM_001099405.2:c.5325G>A
CA352141246
NM_001099405.2:c.5325G>C
CA352141247
NM_001099405.2:c.5325G>T