Canonical Allele Identifier: PA645453723
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 324516
ClinVar RCV Id: RCV000261866 RCV000286707 RCV000317202 RCV000323034 RCV000371794
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Asn1556Ser
CA8708921
NM_000334.4:c.4667A>G