Canonical Allele Identifier: PA2825844441
Gene: SCN4B HGNC NCBI

Linked Data

ClinVar Variation Id: 302646
ClinVar RCV Id: RCV002494949 RCV001549670 RCV003380546 RCV000353970
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135820.1:p.Thr27Arg
CA6300188
NM_001142348.2:c.80C>G