Canonical Allele Identifier: PA2828892837
Gene: CSPP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 510229

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369320.1:p.Glu1099Gly
CA4771124
NM_001382391.1:c.3296A>G