Canonical Allele Identifier: PA2826592593
Gene: CST8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2511487
ClinVar RCV Id: RCV004282544
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268659.1:p.Ser120Arg
CA9789704
NM_001281730.2:c.358A>C
CA9789705
NM_001281730.2:c.360C>G
CA408422435
NM_001281730.2:c.360C>A