Canonical Allele Identifier: PA2826036199
Gene: CTSA HGNC NCBI

Linked Data

ClinVar Variation Id: 380
ClinVar RCV Id: RCV000000411
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161066.2:p.Tyr378Cys
CA114213
NM_001167594.3:c.1133A>G