Allele Registry

Canonical Allele Identifier: PA2580108056

Gene: CTSK HGNC NCBI

ClinVar RCV:

RCV002576733

ClinVar Variation:

1901617

HGVS (amino-acid)	Matching Registered Transcripts
NP_000387.1:p.Lys52Glu	CA342337371 NM_000396.4:c.154A>G