Canonical Allele Identifier: PA2825943239
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 936971
ClinVar RCV Id: RCV003656470

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Glu171Gly
CA352153917
NM_001160161.2:c.512A>G