Canonical Allele Identifier: PA235712
Gene: SCN4B HGNC NCBI

Linked Data

ClinVar Variation Id: 190890
ClinVar RCV Id: RCV000171073 RCV000185523 RCV000619368 RCV001079013 RCV003937533
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_777594.1:p.Gly8Ser
CA235710
NM_174934.4:c.22G>A