Canonical Allele Identifier: PA2825941294
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201481

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Pro950Ser
CA016569
NM_001160160.2:c.2848C>T