Canonical Allele Identifier: PA2827088749
Gene: RAD51AP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2355111
ClinVar RCV Id: RCV004190565
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308162.1:p.Phe856Ser
CA1538811
NM_001321233.1:c.2567T>C