Canonical Allele Identifier: PA264856
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67628
ClinVar RCV Id: RCV000058384 RCV002281902 RCV001569891 RCV001841769 RCV004019029 RCV004528263
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Gly35Ser
CA014210
NM_198056.3:c.103G>A