Canonical Allele Identifier: PA2825939996
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1172409

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Pro52His
CA056571
NM_001160160.2:c.155C>A