Canonical Allele Identifier: PA2573184347
Gene: CTSA HGNC NCBI

Linked Data

ClinVar Variation Id: 1486490
ClinVar RCV Id: RCV002003628
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161066.2:p.Asp31Asn
CA315659009
NM_001167594.3:c.91G>A