Canonical Allele Identifier: PA645453760
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 324507
ClinVar RCV Id: RCV000284690 RCV000279048 RCV000339663 RCV000379267 RCV000517790 RCV000874919
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Ala1765Thr
CA8708788
NM_000334.4:c.5293G>A