Canonical Allele Identifier: PA2827291760
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 192317

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Asn984Lys
CA10575719
NM_001330260.2:c.2952C>G
CA384891868
NM_001330260.2:c.2952C>A