Canonical Allele Identifier: PA2825654324
Gene: CTSA HGNC NCBI

Linked Data

ClinVar Variation Id: 632780
ClinVar RCV Id: RCV000780204 RCV000954191 RCV003334008 RCV003928268
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121167.1:p.Leu19dup
CA9882897
NM_001127695.3:c.54_56dup