Canonical Allele Identifier: PA2827088694
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_001308162.1:p.Ser338Arg
CA1539064
NM_001321233.1:c.1012A>C
CA345916122
NM_001321233.1:c.1014T>G
CA345916128
NM_001321233.1:c.1014T>A