Canonical Allele Identifier: PA2829391837
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 142757
ClinVar RCV Id: RCV000132138 RCV000587595 RCV001038734
ClinVar Variation Id: 2459333
ClinVar RCV Id: RCV003184106 RCV003507485
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Phe8Leu
CA169336
NM_002876.4:c.24T>A
CA400336259
NM_002876.4:c.22T>C
CA400336297
NM_002876.4:c.24T>G