Canonical Allele Identifier: PA2741827774
Gene: RAD51AP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2603292
ClinVar RCV Id: RCV004350330

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092688.1:p.Ile438Leu
CA1539017
NM_001099218.3:c.1312A>C
CA345914380
NM_001099218.3:c.1312A>T