Canonical Allele Identifier: PA2580109064
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 2435741
ClinVar RCV Id: RCV003136491
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Met1619Thr
CA292956828
NM_000334.4:c.4856T>C