Canonical Allele Identifier: PA265563
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67881
ClinVar RCV Id: RCV000058661 RCV000246368 RCV003556154
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Glu1441Gln
CA018141
NM_001099404.2:c.4321G>C