Canonical Allele Identifier: PA2825654323
Gene: CTSA HGNC NCBI

Linked Data

ClinVar Variation Id: 1351603
ClinVar RCV Id: RCV002049270
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121167.1:p.Leu18_Leu19dup
CA9882900
NM_001127695.3:c.51_56dup