Canonical Allele Identifier: PA2827088688
Gene: RAD51AP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2358377
ClinVar RCV Id: RCV004198237
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308162.1:p.Ile313Val
CA1539076
NM_001321233.1:c.937A>G