Canonical Allele Identifier: PA2825115009
Gene: CTSA HGNC NCBI

Linked Data

ClinVar Variation Id: 3078741
ClinVar RCV Id: RCV004375030

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000299.3:p.Glu34Asp
CA9882925
NM_000308.4:c.102G>C
CA409247950
NM_000308.4:c.102G>T