Canonical Allele Identifier: PA2580107758
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 2435729
ClinVar RCV Id: RCV003136479

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Met576Thr
CA400633320
NM_000334.4:c.1727T>C