Canonical Allele Identifier: PA2580107745
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 1985095
ClinVar RCV Id: RCV002780534 RCV003491150
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Pro563Leu
CA8709760
NM_000334.4:c.1688C>T