Canonical Allele Identifier: PA2825654328
Gene: CTSA HGNC NCBI

Linked Data

ClinVar Variation Id: 1406362
ClinVar RCV Id: RCV001935413
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121167.1:p.Leu18Arg
CA9882915
NM_001127695.3:c.53T>G