Canonical Allele Identifier: PA2825942697
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201541
ClinVar Variation Id: 3075439
ClinVar RCV Id: RCV004016957

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Glu1831Asp
CA019360
NM_001160160.2:c.5493G>T
CA352140719
NM_001160160.2:c.5493G>C