Canonical Allele Identifier: PA2829391884
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 1517495

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Pro18Gln
CA400336696
NM_002876.4:c.53C>A