Canonical Allele Identifier: PA2826036017
Gene: CTSA HGNC NCBI

Linked Data

ClinVar Variation Id: 3078741
ClinVar RCV Id: RCV004375030
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161066.2:p.Glu34Asp
CA9882925
NM_001167594.3:c.102G>C
CA409247950
NM_001167594.3:c.102G>T