Canonical Allele Identifier: PA2825844500
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_001135821.1:p.Asp49Glu
CA382777636
NM_001142349.2:c.147C>A
CA382777637
NM_001142349.2:c.147C>G