Canonical Allele Identifier: PA2825943983
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201469
ClinVar RCV Id: RCV000182995
ClinVar Variation Id: 1906128
ClinVar RCV Id: RCV003776596

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Cys683Ser
CA015794
NM_001160161.2:c.2048G>C
CA352144892
NM_001160161.2:c.2047T>A