Canonical Allele Identifier: PA2827088759
Gene: RAD51AP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2233251
ClinVar RCV Id: RCV004094243
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308162.1:p.Phe969Cys
CA43336799
NM_001321233.1:c.2906T>G