Canonical Allele Identifier: PA645460260
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 241774
ClinVar RCV Id: RCV000233856 RCV000506053 RCV000574742
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Phe229Leu
CA10583604
NM_058216.3:c.687C>G
CA400350019
NM_058216.3:c.685T>C
CA400350029
NM_058216.3:c.687C>A