Canonical Allele Identifier: PA299872
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 182830
ClinVar RCV Id: RCV000160918 RCV000198840 RCV000563190 RCV001195011 RCV003462104
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Ile52Leu
CA299870
NM_058216.3:c.154A>C
CA400339550
NM_058216.3:c.154A>T