Allele Registry

Canonical Allele Identifier: PA2828980200

Gene: CTSB HGNC NCBI

ClinVar RCV:

RCV001518415

RCV002161112

RCV003983943

ClinVar Variation:

1168281

1653422

HGVS (amino-acid)	Matching Registered Transcripts
NP_001371652.1:p.Leu26Val	CA4633200 NM_001384723.1:c.76C>G CA2573142567 NM_001384723.1:c.75_76delinsTG