Canonical Allele Identifier: PA913202207
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 628696
ClinVar RCV Id: RCV000773357 RCV000793265 RCV003465693
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Ala139Val
CA400343816
NM_058216.3:c.416C>T