Canonical Allele Identifier: PA2825490578
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 519469

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Ile1612Asn
CA352143128
NM_001099404.2:c.4835T>A