Canonical Allele Identifier: PA2573184356
Gene: CTSA HGNC NCBI

Linked Data

ClinVar Variation Id: 378
ClinVar RCV Id: RCV000000409

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161066.2:p.Trp65Arg
CA114207
NM_001167594.3:c.193T>C
CA409248381
NM_001167594.3:c.193T>A