Canonical Allele Identifier: PA2825654347
Gene: CTSA HGNC NCBI

Linked Data

ClinVar Variation Id: 1360146
ClinVar RCV Id: RCV001864892
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121167.1:p.Leu54Phe
CA9882943
NM_001127695.3:c.160C>T