Canonical Allele Identifier: PA2825115048
Gene: CTSA HGNC NCBI

Linked Data

ClinVar Variation Id: 1512238
ClinVar RCV Id: RCV002022929
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000299.3:p.Pro86Leu
CA409248614
NM_000308.4:c.257C>T