Canonical Allele Identifier: PA2829391912
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 471447
ClinVar RCV Id: RCV000546321 RCV000579909
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Pro21Ala
CA8677134
NM_002876.4:c.61C>G