Allele Registry

Canonical Allele Identifier: PA2573309597

Gene: STT3B HGNC NCBI

ClinVar Allele:

1402631

ClinVar RCV:

RCV001912432

ClinVar Variation:

1392903

HGVS (amino-acid)	Matching Registered Transcripts
NP_849193.1:p.Arg650Gly	CA2295322 NM_178862.3:c.1948A>G