Canonical Allele Identifier: PA2825115377
Gene: CTSA HGNC NCBI

Linked Data

ClinVar Variation Id: 380
ClinVar RCV Id: RCV000000411
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000299.3:p.Tyr395Cys
CA114213
NM_000308.4:c.1184A>G