Canonical Allele Identifier: PA107199
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67843

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Ala1330Pro
CA017704
NM_198056.3:c.3988G>C