Canonical Allele Identifier: PA265667
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67919
ClinVar RCV Id: RCV000058700

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Leu1582Pro
CA018511
NM_198056.3:c.4745T>C