Canonical Allele Identifier: PA107958
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67630
ClinVar RCV Id: RCV000058386

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Gly351Val
CA014246
NM_198056.3:c.1052G>T