Canonical Allele Identifier: PA2825496563
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 519469

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Ile1594Asn
CA352143128
NM_001099405.2:c.4781T>A