Canonical Allele Identifier: PA2827924040
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 919820

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Arg1900His
CA064762
NM_001354701.2:c.5699G>A