Canonical Allele Identifier: PA117795
Gene: RBBP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 5824

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002885.1:p.Lys337Glu
CA117794
NM_002894.3:c.1009A>G