Allele Registry

Canonical Allele Identifier: PA2573299755

Gene: CTSB HGNC NCBI

ClinVar RCV:

RCV001942580

ClinVar Variation:

1365130

HGVS (amino-acid)	Matching Registered Transcripts
NP_680093.1:p.Leu26Met	CA4633202 NM_147783.4:c.76C>A