Canonical Allele Identifier: PA143053
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 48295

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Val924Ile
CA016475
NM_198056.3:c.2770G>A