Canonical Allele Identifier: PA2825115008
Gene: CTSA HGNC NCBI

Linked Data

ClinVar Variation Id: 1489315
ClinVar RCV Id: RCV001980571
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000299.3:p.Asp33Asn
CA409247914
NM_000308.4:c.97G>A