Canonical Allele Identifier: PA287976
Gene: RAD51D HGNC NCBI

Linked Data

ClinVar Variation Id: 127888
ClinVar RCV Id: RCV000649680 RCV000760062 RCV000572128 RCV003321505
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002869.3:p.Asn138His
CA287974
NM_002878.4:c.412A>C