Canonical Allele Identifier: PA199798
Gene: SCN4B HGNC NCBI

Linked Data

ClinVar Variation Id: 191380
ClinVar RCV Id: RCV000171568 RCV000490150 RCV000234662 RCV002354426
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_777594.1:p.Ser206Leu
CA199796
NM_174934.4:c.617C>T