Allele Registry

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Canonical Allele Identifier: PA2825114977

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_000299.3:p.Leu19del	CA201527 NM_000308.4:c.54_56del CA9882916 NM_000308.4:c.55_57del CA10588949 NM_000308.4:c.51_54delinsC