Canonical Allele Identifier: PA1139718456
Gene: CTSD HGNC NCBI

Linked Data

ClinVar Variation Id: 949418

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001900.1:p.Val211Met
CA5814123
NM_001909.5:c.631G>A