Canonical Allele Identifier: PA265696
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67930
ClinVar RCV Id: RCV000058713
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Gln1613Leu
CA018630
NM_198056.3:c.4838A>T