Canonical Allele Identifier: PA2741827770
Gene: RAD51AP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2605925
ClinVar RCV Id: RCV004344580
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092688.1:p.Asp253Tyr
CA1539110
NM_001099218.3:c.757G>T