ClinGen Allele Registry
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Canonical Allele Identifier:
PA915979324
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_001136043.1:p.Asn158His
CA287974
NM_001142571.2:c.472A>C