Canonical Allele Identifier: PA915960894
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 805393
ClinVar RCV Id: RCV000992898 RCV001858758 RCV002479162
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Asp1435His
CA8708996
NM_000334.4:c.4303G>C