Canonical Allele Identifier: PA2825115040
Gene: CTSA HGNC NCBI
ClinVar RCV:
RCV001930359
ClinVar Variation:
1414034
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000299.3:p.Val78Ala
CA315659477
NM_000308.4:c.233T>C