Canonical Allele Identifier: PA658660279
Gene: SCN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 190869
ClinVar RCV Id: RCV000171049 RCV000299875 RCV000254455 RCV000588361 RCV001080647 RCV004539576
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_950238.1:p.Gly10Ser
CA302173
NM_199037.5:c.28G>A