Allele Registry

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Canonical Allele Identifier: PA2830374286

Gene: SCN4B HGNC NCBI

Linked Data

ClinVar Variation Id: 3229289

ClinVar RCV Id: RCV004524867

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_777594.1:p.Asp159Glu	CA382777636 NM_174934.4:c.477C>A CA382777637 NM_174934.4:c.477C>G