Canonical Allele Identifier: PA2825654358
Gene: CTSA HGNC NCBI

Linked Data

ClinVar Variation Id: 1371708
ClinVar RCV Id: RCV001899639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121167.1:p.Asn83Ser
CA9882974
NM_001127695.3:c.248A>G