Canonical Allele Identifier: PA2825494720
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 927132
ClinVar RCV Id: RCV001841102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Ala949Val
CA352140562
NM_001099405.2:c.2846C>T