Canonical Allele Identifier: PA108648
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67949
ClinVar RCV Id: RCV000058734 RCV000190217 RCV000523560 RCV001842375 RCV002336216
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Val1667Ile
CA018825
NM_198056.3:c.4999G>A