Canonical Allele Identifier: PA645453482
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 324531
ClinVar RCV Id: RCV000279770 RCV000299674 RCV000334804 RCV000358171 RCV000576326 RCV000489566 RCV000761997 RCV001084946 RCV004537818
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Pro875Ser
CA8709542
NM_000334.4:c.2623C>T