Canonical Allele Identifier: PA2828078801
Gene: CSPP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 432417

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350061.1:p.Ala1017Val
CA4771112
NM_001363132.2:c.3050C>T