Canonical Allele Identifier: PA208309
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 128211
ClinVar RCV Id: RCV000116180 RCV000515761 RCV000487827 RCV000662625 RCV000709513 RCV000194252 RCV000989962 RCV001270343 RCV001798366 RCV002272129 RCV004528815
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Gly264Ser
CA208307
NM_058216.3:c.790G>A