Canonical Allele Identifier: PA2573168287
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 1367827
ClinVar RCV Id: RCV001947496

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Asp1615Gly
CA400614847
NM_000334.4:c.4844A>G