Canonical Allele Identifier: PA2825654327
Gene: CTSA HGNC NCBI

Linked Data

ClinVar Variation Id: 2825295
ClinVar RCV Id: RCV003599258
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121167.1:p.Leu15Gln
CA9882906
NM_001127695.3:c.44T>A