Canonical Allele Identifier: PA2573168028
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 1479727
ClinVar RCV Id: RCV002009871
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Leu565Val
CA400633586
NM_000334.4:c.1693C>G