Canonical Allele Identifier: PA2828892822
Gene: CSPP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 432417

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369320.1:p.Ala1082Val
CA4771112
NM_001382391.1:c.3245C>T