Canonical Allele Identifier: PA265912
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68034
ClinVar RCV Id: RCV000058837 RCV000454727 RCV001144461 RCV001144462 RCV000987236 RCV001144463 RCV001146371 RCV001146370 RCV001705715 RCV001842408
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Ala226Val
CA019724
NM_000335.5:c.677C>T