Canonical Allele Identifier: PA2827088694
Gene: RAD51AP2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

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