Canonical Allele Identifier: PA2499231297
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 1256463
ClinVar RCV Id: RCV001663805
ClinVar Variation Id: 1503195
ClinVar RCV Id: RCV002045370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Leu1112Phe
CA8709298
NM_000334.4:c.3336G>C
CA400620771
NM_000334.4:c.3336G>T