Allele Registry

Canonical Allele Identifier: PA105522

Gene: SCN4B HGNC NCBI

ClinVar RCV:

RCV000128816

ClinVar Variation:

140600

HGVS (amino-acid)	Matching Registered Transcripts
NP_777594.1:p.Val162Gly	CA163446 NM_174934.4:c.485T>G