Canonical Allele Identifier: PA2580108839
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 1807331
ClinVar RCV Id: RCV002475288
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Leu1433Phe
CA400616283
NM_000334.4:c.4297C>T