Canonical Allele Identifier: PA307439
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201481

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Pro950Ser
CA016569
NM_000335.5:c.2848C>T