Canonical Allele Identifier: PA2830374282
Gene: SCN4B HGNC NCBI

Linked Data

ClinVar Variation Id: 1397893
ClinVar RCV Id: RCV001912656 RCV002334836
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_777594.1:p.Glu157Gln
CA6300191
NM_174934.4:c.469G>C