Canonical Allele Identifier: PA103192
Gene: CTSA HGNC NCBI

Linked Data

ClinVar Variation Id: 377
ClinVar RCV Id: RCV000000408

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121167.1:p.Gln49Arg
CA114204
NM_001127695.3:c.146A>G