Canonical Allele Identifier: PA915971448
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 241771
ClinVar RCV Id: RCV000231632 RCV000582369 RCV003153542
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Trp135Arg
CA10583603
NM_002876.4:c.403T>C
CA400342149
NM_002876.4:c.403T>A