ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA915979236
Gene: RAD51D
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000132446
RCV000476134
RCV003477563
ClinVar Variation:
142955
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001136043.1:p.Gly132Asp
CA169868
NM_001142571.2:c.395G>A