Canonical Allele Identifier: PA645385970
Gene: CTSD HGNC NCBI

Linked Data

ClinVar Variation Id: 303836
ClinVar RCV Id: RCV000320938 RCV001298704
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001900.1:p.Gly316Arg
CA5813993
NM_001909.5:c.946G>A
CA216169761
NM_001909.5:c.946G>C