Canonical Allele Identifier: PA2827088761
Gene: RAD51AP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3151053
ClinVar RCV Id: RCV004445442
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308162.1:p.Glu998Asp
CA345902942
NM_001321233.1:c.2994G>T
CA345902944
NM_001321233.1:c.2994G>C