Canonical Allele Identifier: PA103199
Gene: CTSA HGNC NCBI

Linked Data

ClinVar Variation Id: 385

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121167.1:p.Gly439Ser
CA114224
NM_001127695.3:c.1315G>A