Canonical Allele Identifier: PA107733
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68008

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Gln1909Arg
CA019443
NM_198056.3:c.5726A>G