Canonical Allele Identifier: PA2825114975
Gene: CTSA HGNC NCBI

Linked Data

ClinVar Variation Id: 1351603
ClinVar RCV Id: RCV002049270
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000299.3:p.Leu18_Leu19dup
CA9882900
NM_000308.4:c.51_56dup