Canonical Allele Identifier: PA2825115016
Gene: CTSA HGNC NCBI

Linked Data

ClinVar Variation Id: 569696
ClinVar RCV Id: RCV000690394

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000299.3:p.Pro39Ala
CA409248046
NM_000308.4:c.115C>G