Allele Registry

Canonical Allele Identifier: PA2828980473

Gene: CTSB HGNC NCBI

ClinVar RCV:

RCV001942580

ClinVar Variation:

1365130

HGVS (amino-acid)	Matching Registered Transcripts
NP_001371655.1:p.Leu26Met	CA4633202 NM_001384726.1:c.76C>A