Canonical Allele Identifier: PA2826036021
Gene: CTSA HGNC NCBI

Linked Data

ClinVar Variation Id: 569696
ClinVar RCV Id: RCV000690394

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161066.2:p.Pro39Ala
CA409248046
NM_001167594.3:c.115C>G