Canonical Allele Identifier: PA2825493810
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 834942
ClinVar RCV Id: RCV003541099

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Glu625Asp
CA058996
NM_001099405.2:c.1875G>C
CA352145820
NM_001099405.2:c.1875G>T