Allele Registry

Canonical Allele Identifier: PA103503

Gene: CTSK HGNC NCBI

ClinVar RCV:

RCV000008935

ClinVar Variation:

8424

HGVS (amino-acid)	Matching Registered Transcripts
NP_000387.1:p.Gly79Glu	CA119612 NM_000396.4:c.236G>A