Canonical Allele Identifier: PA307611
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67847
ClinVar RCV Id: RCV000058626 RCV000183057 RCV000456774 RCV004017378
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Ile1334Val
CA017738
NM_198056.3:c.4000A>G