Canonical Allele Identifier: PA2827088722
Gene: RAD51AP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2297953
ClinVar RCV Id: RCV004147510
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308162.1:p.Met702Val
CA345909188
NM_001321233.1:c.2104A>G