Canonical Allele Identifier: PA2825115046
Gene: CTSA HGNC NCBI
ClinVar RCV:
RCV001899639
ClinVar Variation:
1371708
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000299.3:p.Asn83Ser
CA9882974
NM_000308.4:c.248A>G