Canonical Allele Identifier: PA2580142156
Gene: RAD51AP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2258860
ClinVar RCV Id: RCV004117369
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092688.1:p.Ser347Arg
CA1539064
NM_001099218.3:c.1039A>C
CA345916122
NM_001099218.3:c.1041T>G
CA345916128
NM_001099218.3:c.1041T>A