Canonical Allele Identifier: PA2825115032
Gene: CTSA HGNC NCBI
ClinVar RCV:
RCV000000409
ClinVar Variation:
378
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000299.3:p.Trp65Arg
CA114207
NM_000308.4:c.193T>C
CA409248381
NM_000308.4:c.193T>A