Canonical Allele Identifier: PA915971447
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 418441
ClinVar RCV Id: RCV000478459 RCV000566450 RCV000576215 RCV003334388
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Trp135Ser
CA16620494
NM_002876.4:c.404G>C