Canonical Allele Identifier: PA2828157469
Gene: CSPP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 432417

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351798.1:p.Ala1104Val
CA4771112
NM_001364869.1:c.3311C>T