Canonical Allele Identifier: PA277501
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67667

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Arg523Cys
CA014976
NM_198056.3:c.1567C>T