Canonical Allele Identifier: PA2825654339
Gene: CTSA HGNC NCBI

Linked Data

ClinVar Variation Id: 3078741
ClinVar RCV Id: RCV004375030
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121167.1:p.Glu34Asp
CA9882925
NM_001127695.3:c.102G>C
CA409247950
NM_001127695.3:c.102G>T