Canonical Allele Identifier: PA107241
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9381

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Ala1924Thr
CA019460
NM_198056.3:c.5770G>A