Canonical Allele Identifier: PA2825654352
Gene: CTSA HGNC NCBI

Linked Data

ClinVar Variation Id: 2025239
ClinVar RCV Id: RCV002880486
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121167.1:p.Tyr64Ser
CA409248374
NM_001127695.3:c.191A>C