Canonical Allele Identifier: PA2828157635
Gene: CSPP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 446051

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351799.1:p.Lys71Arg
CA4770140
NM_001364870.1:c.212A>G