Canonical Allele Identifier: PA2741815429
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 2573173
ClinVar RCV Id: RCV003315479
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Phe1447Ser
CA400616194
NM_000334.4:c.4340T>C