Canonical Allele Identifier: PA2825130284
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 927132
ClinVar RCV Id: RCV001841102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Ala949Val
CA352140562
NM_000335.5:c.2846C>T