Canonical Allele Identifier: PA330095
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67901

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Met1498Val
CA018339
NM_198056.3:c.4492A>G