Canonical Allele Identifier: PA307698
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67900
ClinVar RCV Id: RCV000058680 RCV000183079
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Tyr1494Ser
CA018330
NM_000335.5:c.4481A>C