Canonical Allele Identifier: PA2829391955
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 372089
ClinVar RCV Id: RCV000410630 RCV000409148 RCV000566177 RCV000780669
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Lys26Met
CA8677141
NM_002876.4:c.77A>T