Canonical Allele Identifier: PA2829393209
Gene: RAD51D HGNC NCBI

Linked Data

ClinVar Variation Id: 1740691
ClinVar RCV Id: RCV002328342
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002869.3:p.Gln148His
CA399089219
NM_002878.4:c.444G>T
CA399089220
NM_002878.4:c.444G>C