Canonical Allele Identifier: PA2825494721
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201481

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Pro950Ser
CA016569
NM_001099405.2:c.2848C>T