Canonical Allele Identifier: PA2573168197
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 1361926
ClinVar RCV Id: RCV001899921
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Met1271Val
CA400617437
NM_000334.4:c.3811A>G