Canonical Allele Identifier: PA2580260974
Gene: CTSD HGNC NCBI

Linked Data

ClinVar Variation Id: 1768172
ClinVar RCV Id: RCV002376778

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001900.1:p.Met326Lys
CA379093407
NM_001909.5:c.977T>A