Canonical Allele Identifier: PA2573184354
Gene: CTSA HGNC NCBI
ClinVar RCV:
RCV001864892
ClinVar Variation:
1360146
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161066.2:p.Leu54Phe
CA9882943
NM_001167594.3:c.160C>T