Canonical Allele Identifier: PA2825115021
Gene: CTSA HGNC NCBI
ClinVar RCV:
RCV001864892
ClinVar Variation:
1360146
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000299.3:p.Leu54Phe
CA9882943
NM_000308.4:c.160C>T