Canonical Allele Identifier: PA108411
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67887

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Ser1458Tyr
CA018188
NM_198056.3:c.4373C>A