Canonical Allele Identifier: PA645506521
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 345111

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Asp2011Glu
CA10618690
NM_198056.3:c.6033C>A
CA352139019
NM_198056.3:c.6033C>G