Canonical Allele Identifier: PA2825942580
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3074125
ClinVar RCV Id: RCV004012667

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Asp1759Glu
CA72937945
NM_001160160.2:c.5277T>A
CA352141253
NM_001160160.2:c.5277T>G