Canonical Allele Identifier: PA2573184326
Gene: CTSA HGNC NCBI

Linked Data

ClinVar Variation Id: 195059
ClinVar RCV Id: RCV000175578 RCV000317016 RCV000588925
ClinVar Variation Id: 266025
ClinVar RCV Id: RCV000256455 RCV003480575
ClinVar Variation Id: 1572689
ClinVar RCV Id: RCV002219943
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161066.2:p.Leu19del
CA201527
NM_001167594.3:c.54_56del
CA9882916
NM_001167594.3:c.55_57del
CA10588949
NM_001167594.3:c.51_54delinsC