Canonical Allele Identifier: PA2499259692
Gene: CTSD HGNC NCBI

Linked Data

ClinVar Variation Id: 1016374
ClinVar RCV Id: RCV001315368

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001900.1:p.Ala410Gly
CA379092320
NM_001909.5:c.1229C>G