Canonical Allele Identifier: PA2825114999
Gene: CTSA HGNC NCBI

Linked Data

ClinVar Variation Id: 952093
ClinVar RCV Id: RCV001224139
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000299.3:p.Ala23Thr
CA409247770
NM_000308.4:c.67G>A