Canonical Allele Identifier: PA915978620
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_001135821.1:p.Ser96Leu
CA199796
NM_001142349.2:c.287C>T