Canonical Allele Identifier: PA341672
Gene: SCN4A HGNC NCBI
ClinVar RCV:
RCV000020272
ClinVar Variation:
21156
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Met1360Val
CA341671
NM_000334.4:c.4078A>G