Canonical Allele Identifier: PA2826794927
Gene: CSPP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 432417

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278268.1:p.Ala732Val
CA4771112
NM_001291339.2:c.2195C>T