Canonical Allele Identifier: PA2741815293
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 2859075
ClinVar RCV Id: RCV003616872
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Ile1110Val
CA400620815
NM_000334.4:c.3328A>G