Canonical Allele Identifier: PA2825492855
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 637989
ClinVar RCV Id: RCV000790455

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Asp356Tyr
CA352149609
NM_001099405.2:c.1066G>T