Canonical Allele Identifier: PA2825844519
Gene: SCN4B HGNC NCBI

Linked Data

ClinVar Variation Id: 190895
ClinVar RCV Id: RCV000994731 RCV001227229 RCV002362871
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135821.1:p.Thr101Arg
CA302222
NM_001142349.2:c.302C>G