Canonical Allele Identifier: PA2825940857
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67696

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Pro637Leu
CA015533
NM_001160160.2:c.1910C>T