Canonical Allele Identifier: PA2828157484
Gene: CSPP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 510229

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351798.1:p.Glu1121Gly
CA4771124
NM_001364869.1:c.3362A>G