Canonical Allele Identifier: PA915978552
Gene: SCN4B HGNC NCBI

Linked Data

ClinVar Variation Id: 190899
ClinVar RCV Id: RCV000171081 RCV002336404 RCV002485078
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135821.1:p.Val42Ile
CA302232
NM_001142349.2:c.124G>A