ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2573184361
Gene: CTSA
HGNC
NCBI
Linked Data
ClinVar Variation Id:
1512238
ClinVar RCV Id:
RCV002022929
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001161066.2:p.Pro86Leu
CA409248614
NM_001167594.3:c.257C>T