Canonical Allele Identifier: PA103270
Gene: CTSA HGNC NCBI

Linked Data

ClinVar Variation Id: 379
ClinVar RCV Id: RCV000000410
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121167.1:p.Ser90Leu
CA114210
NM_001127695.3:c.269C>T
CA2695229839
NM_001127695.3:c.268_269delinsCT