Canonical Allele Identifier: PA2825114976
Gene: CTSA HGNC NCBI

Linked Data

ClinVar Variation Id: 632780
ClinVar RCV Id: RCV000780204 RCV000954191 RCV003334008 RCV003928268
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000299.3:p.Leu19dup
CA9882897
NM_000308.4:c.54_56dup