Canonical Allele Identifier: PA2825115158
Gene: CTSA HGNC NCBI

Linked Data

ClinVar Variation Id: 898718
ClinVar RCV Id: RCV001142771
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000299.3:p.Met192Leu
CA409249605
NM_000308.4:c.574A>C
CA409249609
NM_000308.4:c.574A>T