Canonical Allele Identifier: PA103272
Gene: CTSA HGNC NCBI

Linked Data

ClinVar Variation Id: 378
ClinVar RCV Id: RCV000000409
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121167.1:p.Trp65Arg
CA114207
NM_001127695.3:c.193T>C
CA409248381
NM_001127695.3:c.193T>A