Canonical Allele Identifier: PA2825942281
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 519469

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Ile1579Asn
CA352143128
NM_001160160.2:c.4736T>A