Canonical Allele Identifier: PA2825114969
Gene: CTSA HGNC NCBI

Linked Data

ClinVar Variation Id: 1346626
ClinVar RCV Id: RCV002041453
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000299.3:p.Leu16_Leu19del
CA9882899
NM_000308.4:c.45_56del