Allele Registry

Canonical Allele Identifier: PA100294

Gene: CTSD HGNC NCBI

ClinVar RCV:

RCV000019134

ClinVar Variation:

17573

HGVS (amino-acid)	Matching Registered Transcripts
NP_001900.1:p.Phe229Ile	CA258041 NM_001909.5:c.685T>A