Canonical Allele Identifier: PA2573223751
Gene: CTSD HGNC NCBI
ClinVar RCV:
RCV001908044
ClinVar Variation:
1372517
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001900.1:p.Pro8Ser
CA379101006
NM_001909.5:c.22C>T