Allele Registry

Canonical Allele Identifier: PA915978557

Gene: SCN4B HGNC NCBI

ClinVar RCV:

RCV000128816

ClinVar Variation:

140600

HGVS (amino-acid)	Matching Registered Transcripts
NP_001135821.1:p.Val52Gly	CA163446 NM_001142349.2:c.155T>G