Canonical Allele Identifier: PA2825497686
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 30045

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Asn1969Lys
CA019555
NM_001099405.2:c.5907C>A
CA352139301
NM_001099405.2:c.5907C>G