Canonical Allele Identifier: PA093252
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 5908
ClinVar RCV Id: RCV000153907 RCV000525753 RCV001535772 RCV001799587 RCV002288470
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Gly1306Ala
CA117845
NM_000334.4:c.3917G>C