Canonical Allele Identifier: PA2827922102
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67698
ClinVar RCV Id: RCV000058462 RCV000171572 RCV001842303 RCV003764734 RCV003298119 RCV004528264
ClinVar Variation Id: 67699
ClinVar RCV Id: RCV000058463
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Gly639Arg
CA015554
NM_001354701.2:c.1915G>A
CA015563
NM_001354701.2:c.1915G>C