Canonical Allele Identifier: PA2828158217
Gene: CSPP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 510229

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351799.1:p.Glu1061Gly
CA4771124
NM_001364870.1:c.3182A>G