Canonical Allele Identifier: PA2741815590
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 2729092
ClinVar RCV Id: RCV003506383

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Met1747Thr
CA8708803
NM_000334.4:c.5240T>C