Canonical Allele Identifier: PA2573223811
Gene: CTSD HGNC NCBI

Linked Data

ClinVar Variation Id: 1396731
ClinVar RCV Id: RCV001903138

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001900.1:p.Gly86Arg
CA379098503
NM_001909.5:c.256G>C
CA379098506
NM_001909.5:c.256G>A