Canonical Allele Identifier: PA916017754
Gene: CSPP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 510229

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278268.1:p.Glu749Gly
CA4771124
NM_001291339.2:c.2246A>G