Canonical Allele Identifier: PA2829391915
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 216806
ClinVar RCV Id: RCV000198013 RCV000580606
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Pro21Ser
CA337583
NM_002876.4:c.61C>T