Canonical Allele Identifier: PA2825131276
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 651423
ClinVar RCV Id: RCV003540971

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Leu1341Val
CA352147435
NM_000335.5:c.4021C>G