Canonical Allele Identifier: PA093343
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 661981
ClinVar RCV Id: RCV000992899 RCV000819512 RCV004545804
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Leu1436Pro
CA400616264
NM_000334.4:c.4307T>C