Canonical Allele Identifier: PA645460366
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 409861
ClinVar RCV Id: RCV000567284 RCV000463439 RCV003105914
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Phe339Ser
CA16615808
NM_058216.3:c.1016T>C