Canonical Allele Identifier: PA2827088702
Gene: RAD51AP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2603292
ClinVar RCV Id: RCV004350330
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308162.1:p.Ile429Leu
CA1539017
NM_001321233.1:c.1285A>C
CA345914380
NM_001321233.1:c.1285A>T