Canonical Allele Identifier: PA339594
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 216803
ClinVar RCV Id: RCV000200867 RCV000484571 RCV000569780 RCV001798673 RCV003462343
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Glu36Lys
CA339592
NM_058216.3:c.106G>A