Canonical Allele Identifier: PA658668954
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 448282
ClinVar RCV Id: RCV000516982
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Leu1489Phe
CA400615968
NM_000334.4:c.4465C>T