Allele Registry

Canonical Allele Identifier: PA2573168949

Gene: CTSK HGNC NCBI

ClinVar RCV:

RCV001908894

RCV002482795

ClinVar Variation:

1403119

HGVS (amino-acid)	Matching Registered Transcripts
NP_000387.1:p.Asp272Asn	CA1080418 NM_000396.4:c.814G>A