Canonical Allele Identifier: PA2825115052
Gene: CTSA HGNC NCBI

Linked Data

ClinVar Variation Id: 932379
ClinVar RCV Id: RCV001200149

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000299.3:p.Ser89Arg
CA409248629
NM_000308.4:c.265A>C
CA409248635
NM_000308.4:c.267C>A
CA409248636
NM_000308.4:c.267C>G