Canonical Allele Identifier: PA2825497093
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3074125
ClinVar RCV Id: RCV004012667

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Asp1774Glu
CA72937945
NM_001099405.2:c.5322T>A
CA352141253
NM_001099405.2:c.5322T>G