Canonical Allele Identifier: PA2825497245
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 628397
ClinVar RCV Id: RCV001841889
ClinVar Variation Id: 2200145
ClinVar RCV Id: RCV003542438

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Val1825Leu
CA352140920
NM_001099405.2:c.5473G>T
CA352140921
NM_001099405.2:c.5473G>C