Canonical Allele Identifier: PA2825495420
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 935348
ClinVar RCV Id: RCV003656456

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Ala1186Asp
CA352138211
NM_001099405.2:c.3557C>A