Canonical Allele Identifier: PA2499255299
Gene: CUL7 HGNC NCBI

Linked Data

ClinVar Variation Id: 999261
ClinVar RCV Id: RCV001295235

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361801.1:p.Ser397Arg
CA3814237
NM_001374872.1:c.1189A>C
CA364227232
NM_001374872.1:c.1191T>G
CA364227234
NM_001374872.1:c.1191T>A