Canonical Allele Identifier: PA1139677378
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 864440
ClinVar RCV Id: RCV001071629 RCV003142033
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Thr585Ala
CA400633163
NM_000334.4:c.1753A>G