Canonical Allele Identifier: PA916043659
Gene: CSPP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 432417
ClinVar RCV Id: RCV000498042 RCV002524083
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350062.1:p.Ala990Val
CA4771112
NM_001363133.2:c.2969C>T