Canonical Allele Identifier: PA1139678641
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 854406

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Thr1605Ile
CA400614914
NM_000334.4:c.4814C>T