Canonical Allele Identifier: PA2825943815
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 927347
ClinVar RCV Id: RCV001841109

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Gln575Glu
CA352146502
NM_001160161.2:c.1723C>G