Canonical Allele Identifier: PA2825944812
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2760216
ClinVar RCV Id: RCV003572060

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Leu1248Pro
CA352148161
NM_001160161.2:c.3743T>C