Canonical Allele Identifier: PA2825495877
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 651423
ClinVar RCV Id: RCV003540971

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Leu1342Val
CA352147435
NM_001099405.2:c.4024C>G