Allele Registry

Canonical Allele Identifier: PA916025084

Gene: SCN1B HGNC NCBI

ClinVar RCV:

RCV000416448

ClinVar Variation:

375404

HGVS (amino-acid)	Matching Registered Transcripts
NP_001308534.1:p.Asp70Val	CA16044237 NM_001321605.1:c.209A>T