Canonical Allele Identifier: PA249884
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9406

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Asp1594His
CA018558
NM_000335.5:c.4780G>C