Canonical Allele Identifier: PA2829392252
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 484739
ClinVar RCV Id: RCV000568378 RCV001853743
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.His82Gln
CA400340351
NM_002876.4:c.246C>A
CA400340355
NM_002876.4:c.246C>G