Canonical Allele Identifier: PA093223
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 5922
ClinVar RCV Id: RCV000006285 RCV003996078
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Asn1297Lys
CA117854
NM_000334.4:c.3891C>A
CA400617259
NM_000334.4:c.3891C>G