Canonical Allele Identifier: PA2580555237
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2146111

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.His617Arg
CA352145914
NM_198056.3:c.1850A>G