Canonical Allele Identifier: PA249885
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9406

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Asp1595His
CA018558
NM_001099404.2:c.4783G>C