Canonical Allele Identifier: PA155076
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 130233
ClinVar RCV Id: RCV000118269 RCV000289506 RCV000390854 RCV000351508 RCV000392527 RCV000811377 RCV003488392
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Glu1202Lys
CA155075
NM_000334.4:c.3604G>A